Canonical Allele Identifier: CA99712021

Gene: ALB

Linked Data

• dbSNP Id: rs11538208
• MyVariant Identifiers: chr4:g.74285286T>A (hg19) ; chr4:g.73419569T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419569T>A , CM000666.2:g.73419569T>A	GRCh38
NC_000004.11:g.74285286T>A , CM000666.1:g.74285286T>A	GRCh37
NC_000004.10:g.74504150T>A	NCBI36
NG_009291.1:g.20315T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1715T>A MANE Select	ENSP00000295897.4:p.Met572Lys
ENST00000295897.8:c.1715T>A	ENSP00000295897.4:p.Met572Lys
ENST00000401494.7:c.1370T>A	ENSP00000384695.3:p.Met457Lys
ENST00000415165.6:c.1139T>A	ENSP00000401820.2:p.Met380Lys
ENST00000476441.6:c.*994T>A	ENSP00000423727.1:n.*994T>A
ENST00000495173.1:n.23T>A
ENST00000503124.5:c.1265T>A	ENSP00000421027.1:p.Met422Lys
ENST00000505649.5:n.1262T>A
ENST00000508932.5:n.175+114T>A
ENST00000509063.5:c.1715T>A	ENSP00000422784.1:p.Met572Lys
ENST00000511370.1:c.1248T>A
ENST00000621085.4:c.1076T>A	ENSP00000483421.1:p.Met359Lys
ENST00000621628.4:c.1076T>A	ENSP00000480485.1:p.Met359Lys
NM_000477.5:c.1715T>A	NP_000468.1:p.Met572Lys
NM_000477.6:c.1715T>A	NP_000468.1:p.Met572Lys
NM_000477.7:c.1715T>A MANE Select	NP_000468.1:p.Met572Lys