Canonical Allele Identifier: CA913046848

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100380945_100380947del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99915389_99915391del , CM000663.2:g.99915389_99915391del	GRCh38
NC_000001.10:g.100380945_100380947del , CM000663.1:g.100380945_100380947del	GRCh37
NC_000001.9:g.100153533_100153535del	NCBI36
NG_012865.1:g.70306_70308del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4162_4164del MANE Select	ENSP00000355106.3:p.Ala1388del
ENST00000637337.1:n.4373_4375del
ENST00000294724.8:c.4162_4164del	ENSP00000294724.4:p.Ala1388del
ENST00000361302.7:c.4114_4116del	ENSP00000354971.3:p.Ala1372del
ENST00000361522.4:c.4111_4113del	ENSP00000354635.4:p.Ala1371del
ENST00000361915.7:c.4162_4164del	ENSP00000355106.3:p.Ala1388del
ENST00000370161.6:c.4114_4116del	ENSP00000359180.2:p.Ala1372del
ENST00000370163.7:c.4162_4164del	ENSP00000359182.3:p.Ala1388del
ENST00000370165.7:c.4162_4164del	ENSP00000359184.3:p.Ala1388del
NM_000028.2:c.4162_4164del	NP_000019.2:p.Ala1388del
NM_000642.2:c.4162_4164del	NP_000633.2:p.Ala1388del
NM_000643.2:c.4162_4164del	NP_000634.2:p.Ala1388del
NM_000644.2:c.4162_4164del	NP_000635.2:p.Ala1388del
NM_000645.2:c.4111_4113del	NP_000636.2:p.Ala1371del
NM_000646.2:c.4114_4116del	NP_000637.2:p.Ala1372del
XM_005270557.1:c.4162_4164del	XP_005270614.1:p.Ala1388del
XR_947626.1:n.1318-2174_1318-2172del
XR_947627.1:n.1207-2174_1207-2172del
XR_947628.1:n.1312-2174_1312-2172del
XR_947630.1:n.1250-2174_1250-2172del
XR_947632.1:n.1136-2174_1136-2172del
XR_947633.1:n.1247-2174_1247-2172del
XR_947634.1:n.661-2174_661-2172del
XR_947635.1:n.729-2174_729-2172del
XM_005270557.2:c.4162_4164del	XP_005270614.1:p.Ala1388del
XM_017000501.2:c.2422_2424del	XP_016855990.1:p.Ala808del
NM_000642.3:c.4162_4164del MANE Select	NP_000633.2:p.Ala1388del