Canonical Allele Identifier: CA2646736026

Gene: AGL

Linked Data

• gnomAD v4: 1-99850932-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99850932G>T , CM000663.2:g.99850932G>T	GRCh38
NC_000001.10:g.100316488G>T , CM000663.1:g.100316488G>T	GRCh37
NC_000001.9:g.100089076G>T	NCBI36
NG_012865.1:g.5849G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.-68-43G>T MANE Select	ENSP00000355106.3:n.-68-43G>T
ENST00000294724.8:c.-69+34G>T	ENSP00000294724.4:n.-69+34G>T
ENST00000361915.7:c.-68-43G>T	ENSP00000355106.3:n.-68-43G>T
ENST00000370163.7:c.-68-43G>T	ENSP00000359182.3:n.-68-43G>T
ENST00000370165.7:c.-8-103G>T	ENSP00000359184.3:n.-8-103G>T
NM_000028.2:c.-69+34G>T	NP_000019.2:n.-69+34G>T
NM_000642.2:c.-68-43G>T	NP_000633.2:n.-68-43G>T
NM_000643.2:c.-68-43G>T	NP_000634.2:n.-68-43G>T
NM_000644.2:c.-8-103G>T	NP_000635.2:n.-8-103G>T
XM_005270557.1:c.-68-43G>T	XP_005270614.1:n.-68-43G>T
XM_005270557.2:c.-68-43G>T	XP_005270614.1:n.-68-43G>T
NM_000642.3:c.-68-43G>T MANE Select	NP_000633.2:n.-68-43G>T