Canonical Allele Identifier: CA357247117

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285984T>C (hg19) ; chr4:g.73420267T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420267T>C , CM000666.2:g.73420267T>C	GRCh38
NC_000004.11:g.74285984T>C , CM000666.1:g.74285984T>C	GRCh37
NC_000004.10:g.74504848T>C	NCBI36
NG_009291.1:g.21013T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1799T>C MANE Select	ENSP00000295897.4:p.Val600Ala
ENST00000295897.8:c.1799T>C	ENSP00000295897.4:p.Val600Ala
ENST00000401494.7:c.1454T>C	ENSP00000384695.3:p.Val485Ala
ENST00000415165.6:c.1223T>C	ENSP00000401820.2:p.Val408Ala
ENST00000476441.6:c.*1078T>C	ENSP00000423727.1:n.*1078T>C
ENST00000495173.1:n.107T>C
ENST00000503124.5:c.1349T>C	ENSP00000421027.1:p.Val450Ala
ENST00000505649.5:n.1346T>C
ENST00000508932.5:n.189T>C
ENST00000509063.5:c.1785+628T>C	ENSP00000422784.1:n.1785+628T>C
ENST00000511370.1:c.1332T>C
ENST00000621085.4:c.1160T>C	ENSP00000483421.1:p.Val387Ala
ENST00000621628.4:c.1160T>C	ENSP00000480485.1:p.Val387Ala
NM_000477.5:c.1799T>C	NP_000468.1:p.Val600Ala
NM_000477.6:c.1799T>C	NP_000468.1:p.Val600Ala
NM_000477.7:c.1799T>C MANE Select	NP_000468.1:p.Val600Ala