Canonical Allele Identifier: CA2325644664

Gene: CPAMD8

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17007575_17007579delinsAGGAG , CM000681.2:g.17007575_17007579delinsAGGAG	GRCh38
NC_000019.9:g.17118385_17118389delinsAGGAG , CM000681.1:g.17118385_17118389delinsAGGAG	GRCh37
NC_000019.8:g.16979385_16979389delinsAGGAG	NCBI36
NG_054892.1:g.24240_24244delinsCTCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000651564.2:c.559+926_559+930delinsCTCCT	ENSP00000498697.2:n.559+926_559+930delinsCTCCT
ENST00000291440.4:c.559+926_559+930delinsCTCCT	ENSP00000291440.4:n.559+926_559+930delinsCTCCT
ENST00000443236.7:c.559+926_559+930delinsCTCCT MANE Select	ENSP00000402505.3:n.559+926_559+930delinsCTCCT
ENST00000651564.1:c.700+926_700+930delinsCTCCT	ENSP00000498697.1:n.700+926_700+930delinsCTCCT
ENST00000291440.3:c.700+926_700+930delinsCTCCT	ENSP00000291440.3:n.700+926_700+930delinsCTCCT
ENST00000388925.8:c.559+926_559+930delinsCTCCT	ENSP00000373577.4:n.559+926_559+930delinsCTCCT
ENST00000443236.5:c.700+926_700+930delinsCTCCT	ENSP00000402505.2:n.700+926_700+930delinsCTCCT
NM_015692.2:c.700+926_700+930delinsCTCCT	NP_056507.2:n.700+926_700+930delinsCTCCT
XM_011527917.1:c.664+926_664+930delinsCTCCT	XP_011526219.1:n.664+926_664+930delinsCTCCT
XM_011527918.1:c.700+926_700+930delinsCTCCT	XP_011526220.1:n.700+926_700+930delinsCTCCT
XM_011527919.1:c.700+926_700+930delinsCTCCT	XP_011526221.1:n.700+926_700+930delinsCTCCT
XM_011527920.1:c.700+926_700+930delinsCTCCT	XP_011526222.1:n.700+926_700+930delinsCTCCT
XM_011527921.1:c.700+926_700+930delinsCTCCT	XP_011526223.1:n.700+926_700+930delinsCTCCT
XM_011527922.1:c.700+926_700+930delinsCTCCT	XP_011526224.1:n.700+926_700+930delinsCTCCT
XM_011527923.1:c.700+926_700+930delinsCTCCT	XP_011526225.1:n.700+926_700+930delinsCTCCT
XM_011527924.1:c.700+926_700+930delinsCTCCT	XP_011526226.1:n.700+926_700+930delinsCTCCT
NM_015692.4:c.559+926_559+930delinsCTCCT	NP_056507.3:n.559+926_559+930delinsCTCCT
XM_011527920.2:c.700+926_700+930delinsCTCCT	XP_011526222.1:n.700+926_700+930delinsCTCCT
XM_011527921.3:c.700+926_700+930delinsCTCCT	XP_011526223.1:n.700+926_700+930delinsCTCCT
XM_011527924.2:c.700+926_700+930delinsCTCCT	XP_011526226.1:n.700+926_700+930delinsCTCCT
XM_017026594.1:c.700+926_700+930delinsCTCCT	XP_016882083.1:n.700+926_700+930delinsCTCCT
NM_015692.5:c.559+926_559+930delinsCTCCT MANE Select	NP_056507.3:n.559+926_559+930delinsCTCCT
NR_165644.1:n.727+926_727+930delinsCTCCT