Canonical Allele Identifier: CA341342646

Gene: AGL

Linked Data

• gnomAD v4: 1-99916719-T-C
• MyVariant Identifiers: chr1:g.100382275T>C (hg19) ; chr1:g.99916719T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916719T>C , CM000663.2:g.99916719T>C	GRCh38
NC_000001.10:g.100382275T>C , CM000663.1:g.100382275T>C	GRCh37
NC_000001.9:g.100154863T>C	NCBI36
NG_012865.1:g.71636T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4469T>C MANE Select	ENSP00000355106.3:p.Val1490Ala
ENST00000637337.1:n.4680T>C
ENST00000294724.8:c.4469T>C	ENSP00000294724.4:p.Val1490Ala
ENST00000361302.7:c.4421T>C	ENSP00000354971.3:p.Val1474Ala
ENST00000361522.4:c.4418T>C	ENSP00000354635.4:p.Val1473Ala
ENST00000361915.7:c.4469T>C	ENSP00000355106.3:p.Val1490Ala
ENST00000370161.6:c.4421T>C	ENSP00000359180.2:p.Val1474Ala
ENST00000370163.7:c.4469T>C	ENSP00000359182.3:p.Val1490Ala
ENST00000370165.7:c.4469T>C	ENSP00000359184.3:p.Val1490Ala
NM_000028.2:c.4469T>C	NP_000019.2:p.Val1490Ala
NM_000642.2:c.4469T>C	NP_000633.2:p.Val1490Ala
NM_000643.2:c.4469T>C	NP_000634.2:p.Val1490Ala
NM_000644.2:c.4469T>C	NP_000635.2:p.Val1490Ala
NM_000645.2:c.4418T>C	NP_000636.2:p.Val1473Ala
NM_000646.2:c.4421T>C	NP_000637.2:p.Val1474Ala
XM_005270557.1:c.4469T>C	XP_005270614.1:p.Val1490Ala
XR_947626.1:n.1318-3502A>G
XR_947627.1:n.1207-3502A>G
XR_947628.1:n.1312-3502A>G
XR_947630.1:n.1250-3502A>G
XR_947632.1:n.1136-3502A>G
XR_947633.1:n.1247-3502A>G
XR_947634.1:n.661-3502A>G
XR_947635.1:n.729-3502A>G
XM_005270557.2:c.4469T>C	XP_005270614.1:p.Val1490Ala
XM_017000501.2:c.2729T>C	XP_016855990.1:p.Val910Ala
NM_000642.3:c.4469T>C MANE Select	NP_000633.2:p.Val1490Ala