Canonical Allele Identifier: CA2479570690

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406481_151406486delinsCAAAGA , CM000663.2:g.151406481_151406486delinsCAAAGA	GRCh38
NC_000001.10:g.151378957_151378962delinsCAAAGA , CM000663.1:g.151378957_151378962delinsCAAAGA	GRCh37
NC_000001.9:g.149645581_149645586delinsCAAAGA	NCBI36
NG_046601.1:g.57980_57985delinsTCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2619-22_2619-17delinsTCTTTG	ENSP00000518163.1:n.2619-22_2619-17delinsTCTTTG
ENST00000392723.6:c.2412-22_2412-17delinsTCTTTG	ENSP00000376484.1:n.2412-22_2412-17delinsTCTTTG
ENST00000439756.2:c.2571-22_2571-17delinsTCTTTG	ENSP00000390156.2:n.2571-22_2571-17delinsTCTTTG
ENST00000703168.1:c.2592-22_2592-17delinsTCTTTG	ENSP00000515214.1:n.2592-22_2592-17delinsTCTTTG
ENST00000271715.7:c.2571-22_2571-17delinsTCTTTG MANE Select	ENSP00000271715.2:n.2571-22_2571-17delinsTCTTTG
ENST00000271715.6:c.2571-22_2571-17delinsTCTTTG	ENSP00000271715.2:n.2571-22_2571-17delinsTCTTTG
ENST00000358476.7:n.2719-22_2719-17delinsTCTTTG
ENST00000368863.6:c.2286-22_2286-17delinsTCTTTG	ENSP00000357856.2:n.2286-22_2286-17delinsTCTTTG
ENST00000392723.5:c.2412-22_2412-17delinsTCTTTG	ENSP00000376484.1:n.2412-22_2412-17delinsTCTTTG
ENST00000409503.5:c.2544-22_2544-17delinsTCTTTG	ENSP00000386836.1:n.2544-22_2544-17delinsTCTTTG
ENST00000491586.5:c.2439-22_2439-17delinsTCTTTG	ENSP00000418408.1:n.2439-22_2439-17delinsTCTTTG
ENST00000529669.1:c.771-22_771-17delinsTCTTTG	ENSP00000432295.1:n.771-22_771-17delinsTCTTTG
ENST00000531094.5:c.2385-22_2385-17delinsTCTTTG	ENSP00000431259.1:n.2385-22_2385-17delinsTCTTTG
NM_001194937.1:c.2544-22_2544-17delinsTCTTTG	NP_001181866.1:n.2544-22_2544-17delinsTCTTTG
NM_001194938.1:c.2385-22_2385-17delinsTCTTTG	NP_001181867.1:n.2385-22_2385-17delinsTCTTTG
NM_015100.3:c.2571-22_2571-17delinsTCTTTG	NP_055915.2:n.2571-22_2571-17delinsTCTTTG
NM_145796.3:c.2286-22_2286-17delinsTCTTTG	NP_665739.3:n.2286-22_2286-17delinsTCTTTG
NM_207171.2:c.2412-22_2412-17delinsTCTTTG	NP_997054.1:n.2412-22_2412-17delinsTCTTTG
XM_005244999.1:c.2571-22_2571-17delinsTCTTTG	XP_005245056.1:n.2571-22_2571-17delinsTCTTTG
XM_005245000.3:c.2571-22_2571-17delinsTCTTTG	XP_005245057.1:n.2571-22_2571-17delinsTCTTTG
XM_005245001.1:c.2571-22_2571-17delinsTCTTTG	XP_005245058.1:n.2571-22_2571-17delinsTCTTTG
XM_005245005.1:c.2412-22_2412-17delinsTCTTTG	XP_005245062.1:n.2412-22_2412-17delinsTCTTTG
XM_005245006.3:c.2412-22_2412-17delinsTCTTTG	XP_005245063.1:n.2412-22_2412-17delinsTCTTTG
XM_011509330.1:c.2463-22_2463-17delinsTCTTTG	XP_011507632.1:n.2463-22_2463-17delinsTCTTTG
XM_011509331.1:c.2214-22_2214-17delinsTCTTTG	XP_011507633.1:n.2214-22_2214-17delinsTCTTTG
XR_921760.1:n.2399-22_2399-17delinsTCTTTG
XM_005244999.3:c.2571-22_2571-17delinsTCTTTG	XP_005245056.1:n.2571-22_2571-17delinsTCTTTG
XM_005245000.4:c.2571-22_2571-17delinsTCTTTG	XP_005245057.1:n.2571-22_2571-17delinsTCTTTG
XM_005245001.2:c.2571-22_2571-17delinsTCTTTG	XP_005245058.1:n.2571-22_2571-17delinsTCTTTG
XM_005245005.2:c.2412-22_2412-17delinsTCTTTG	XP_005245062.1:n.2412-22_2412-17delinsTCTTTG
XM_005245006.5:c.2412-22_2412-17delinsTCTTTG	XP_005245063.1:n.2412-22_2412-17delinsTCTTTG
XM_017000744.1:c.2592-22_2592-17delinsTCTTTG	XP_016856233.1:n.2592-22_2592-17delinsTCTTTG
XM_017000745.2:c.2544-22_2544-17delinsTCTTTG	XP_016856234.1:n.2544-22_2544-17delinsTCTTTG
XM_017000746.1:c.2544-22_2544-17delinsTCTTTG	XP_016856235.1:n.2544-22_2544-17delinsTCTTTG
XM_017000748.1:c.2412-22_2412-17delinsTCTTTG	XP_016856237.1:n.2412-22_2412-17delinsTCTTTG
XM_017000749.1:c.2412-22_2412-17delinsTCTTTG	XP_016856238.1:n.2412-22_2412-17delinsTCTTTG
XM_024454305.1:c.2445-22_2445-17delinsTCTTTG	XP_024310073.1:n.2445-22_2445-17delinsTCTTTG
XM_024454306.1:c.1371-22_1371-17delinsTCTTTG	XP_024310074.1:n.1371-22_1371-17delinsTCTTTG
XR_002959801.1:n.2426-22_2426-17delinsTCTTTG
NM_015100.4:c.2571-22_2571-17delinsTCTTTG MANE Select	NP_055915.2:n.2571-22_2571-17delinsTCTTTG
NM_001194937.2:c.2544-22_2544-17delinsTCTTTG	NP_001181866.1:n.2544-22_2544-17delinsTCTTTG
NM_001194938.2:c.2385-22_2385-17delinsTCTTTG	NP_001181867.1:n.2385-22_2385-17delinsTCTTTG
NM_145796.4:c.2286-22_2286-17delinsTCTTTG	NP_665739.3:n.2286-22_2286-17delinsTCTTTG