Canonical Allele Identifier: CA2646739606

Gene: AGL

Linked Data

• gnomAD v4: 1-99921762-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921762T>C , CM000663.2:g.99921762T>C	GRCh38
NC_000001.10:g.100387318T>C , CM000663.1:g.100387318T>C	GRCh37
NC_000001.9:g.100159906T>C	NCBI36
NG_012865.1:g.76679T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*111T>C MANE Select	ENSP00000355106.3:n.*111T>C
ENST00000637337.1:n.4921T>C
ENST00000294724.8:c.*111T>C	ENSP00000294724.4:n.*111T>C
ENST00000361302.7:c.*111T>C	ENSP00000354971.3:n.*111T>C
ENST00000361522.4:c.*111T>C	ENSP00000354635.4:n.*111T>C
ENST00000361915.7:c.*111T>C	ENSP00000355106.3:n.*111T>C
ENST00000370161.6:c.4662T>C	ENSP00000359180.2:n.4662T>C
ENST00000370163.7:c.*111T>C	ENSP00000359182.3:n.*111T>C
ENST00000370165.7:c.*111T>C	ENSP00000359184.3:n.*111T>C
NM_000028.2:c.*111T>C	NP_000019.2:n.*111T>C
NM_000642.2:c.*111T>C	NP_000633.2:n.*111T>C
NM_000643.2:c.*111T>C	NP_000634.2:n.*111T>C
NM_000644.2:c.*111T>C	NP_000635.2:n.*111T>C
NM_000645.2:c.*111T>C	NP_000636.2:n.*111T>C
NM_000646.2:c.*111T>C	NP_000637.2:n.*111T>C
XM_005270557.1:c.*111T>C	XP_005270614.1:n.*111T>C
XR_947626.1:n.1317+2476A>G
XR_947627.1:n.1206+2476A>G
XR_947628.1:n.1311+2476A>G
XR_947630.1:n.1249+2476A>G
XR_947632.1:n.1135+2476A>G
XR_947633.1:n.1246+2476A>G
XR_947634.1:n.660+2476A>G
XR_947635.1:n.728+2476A>G
XM_005270557.2:c.*111T>C	XP_005270614.1:n.*111T>C
XM_017000501.2:c.*111T>C	XP_016855990.1:n.*111T>C
NM_000642.3:c.*111T>C MANE Select	NP_000633.2:n.*111T>C