Canonical Allele Identifier: CA341323342

Gene: AGL

Linked Data

• gnomAD v4: 1-99851044-T-C
• MyVariant Identifiers: chr1:g.100316600T>C (hg19) ; chr1:g.99851044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99851044T>C , CM000663.2:g.99851044T>C	GRCh38
NC_000001.10:g.100316600T>C , CM000663.1:g.100316600T>C	GRCh37
NC_000001.9:g.100089188T>C	NCBI36
NG_012865.1:g.5961T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.2T>C MANE Select	ENSP00000355106.3:p.Met1Thr
ENST00000294724.8:c.2T>C	ENSP00000294724.4:p.Met1Thr
ENST00000361302.7:c.-190T>C	ENSP00000354971.3:n.-190T>C
ENST00000361915.7:c.2T>C	ENSP00000355106.3:p.Met1Thr
ENST00000370163.7:c.2T>C	ENSP00000359182.3:p.Met1Thr
ENST00000370165.7:c.2T>C	ENSP00000359184.3:p.Met1Thr
NM_000028.2:c.2T>C	NP_000019.2:p.Met1Thr
NM_000642.2:c.2T>C	NP_000633.2:p.Met1Thr
NM_000643.2:c.2T>C	NP_000634.2:p.Met1Thr
NM_000644.2:c.2T>C	NP_000635.2:p.Met1Thr
NM_000646.2:c.-190T>C	NP_000637.2:n.-190T>C
XM_005270557.1:c.2T>C	XP_005270614.1:p.Met1Thr
XM_005270557.2:c.2T>C	XP_005270614.1:p.Met1Thr
NM_000642.3:c.2T>C MANE Select	NP_000633.2:p.Met1Thr