Canonical Allele Identifier: CA357238117

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275115C>A (hg19) ; chr4:g.73409398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409398C>A , CM000666.2:g.73409398C>A	GRCh38
NC_000004.11:g.74275115C>A , CM000666.1:g.74275115C>A	GRCh37
NC_000004.10:g.74493979C>A	NCBI36
NG_009291.1:g.10144C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.526C>A MANE Select	ENSP00000295897.4:p.Pro176Thr
ENST00000295897.8:c.526C>A	ENSP00000295897.4:p.Pro176Thr
ENST00000401494.7:c.181C>A	ENSP00000384695.3:p.Pro61Thr
ENST00000415165.6:c.138-2598C>A	ENSP00000401820.2:n.138-2598C>A
ENST00000441319.5:c.532C>A	ENSP00000392541.1:p.Pro178Thr
ENST00000476441.6:c.123C>A	ENSP00000423727.1:p.Pro41=
ENST00000503124.5:c.76C>A	ENSP00000421027.1:p.Pro26Thr
ENST00000505649.5:n.212C>A
ENST00000509063.5:c.526C>A	ENSP00000422784.1:p.Pro176Thr
ENST00000511370.1:c.59C>A
ENST00000514786.1:n.495C>A
ENST00000621085.4:c.490+36C>A	ENSP00000483421.1:n.490+36C>A
ENST00000621628.4:c.486+322C>A	ENSP00000480485.1:n.486+322C>A
NM_000477.5:c.526C>A	NP_000468.1:p.Pro176Thr
NM_000477.6:c.526C>A	NP_000468.1:p.Pro176Thr
NM_000477.7:c.526C>A MANE Select	NP_000468.1:p.Pro176Thr