Canonical Allele Identifier: CA357241425

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280849G>A (hg19) ; chr4:g.73415132G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415132G>A , CM000666.2:g.73415132G>A	GRCh38
NC_000004.11:g.74280849G>A , CM000666.1:g.74280849G>A	GRCh37
NC_000004.10:g.74499713G>A	NCBI36
NG_009291.1:g.15878G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1156G>A MANE Select	ENSP00000295897.4:p.Ala386Thr
ENST00000295897.8:c.1156G>A	ENSP00000295897.4:p.Ala386Thr
ENST00000401494.7:c.811G>A	ENSP00000384695.3:p.Ala271Thr
ENST00000415165.6:c.580G>A	ENSP00000401820.2:p.Ala194Thr
ENST00000476441.6:c.*435G>A	ENSP00000423727.1:n.*435G>A
ENST00000484992.1:n.476G>A
ENST00000503124.5:c.706G>A	ENSP00000421027.1:p.Ala236Thr
ENST00000504043.1:n.159G>A
ENST00000505649.5:n.842G>A
ENST00000509063.5:c.1156G>A	ENSP00000422784.1:p.Ala386Thr
ENST00000511370.1:c.689G>A
ENST00000621085.4:c.517G>A	ENSP00000483421.1:p.Ala173Thr
ENST00000621628.4:c.517G>A	ENSP00000480485.1:p.Ala173Thr
NM_000477.5:c.1156G>A	NP_000468.1:p.Ala386Thr
NM_000477.6:c.1156G>A	NP_000468.1:p.Ala386Thr
NM_000477.7:c.1156G>A MANE Select	NP_000468.1:p.Ala386Thr