Canonical Allele Identifier: CA439800354

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280857A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415140A>C , CM000666.2:g.73415140A>C	GRCh38
NC_000004.11:g.74280857A>C , CM000666.1:g.74280857A>C	GRCh37
NC_000004.10:g.74499721A>C	NCBI36
NG_009291.1:g.15886A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1164A>C MANE Select	ENSP00000295897.4:p.Ala388=
ENST00000295897.8:c.1164A>C	ENSP00000295897.4:p.Ala388=
ENST00000401494.7:c.819A>C	ENSP00000384695.3:p.Ala273=
ENST00000415165.6:c.588A>C	ENSP00000401820.2:p.Ala196=
ENST00000476441.6:c.*443A>C	ENSP00000423727.1:n.*443A>C
ENST00000484992.1:n.484A>C
ENST00000503124.5:c.714A>C	ENSP00000421027.1:p.Ala238=
ENST00000504043.1:n.167A>C
ENST00000505649.5:n.850A>C
ENST00000509063.5:c.1164A>C	ENSP00000422784.1:p.Ala388=
ENST00000511370.1:c.697A>C
ENST00000621085.4:c.525A>C	ENSP00000483421.1:p.Ala175=
ENST00000621628.4:c.525A>C	ENSP00000480485.1:p.Ala175=
NM_000477.5:c.1164A>C	NP_000468.1:p.Ala388=
NM_000477.6:c.1164A>C	NP_000468.1:p.Ala388=
NM_000477.7:c.1164A>C MANE Select	NP_000468.1:p.Ala388=