Canonical Allele Identifier: CA439798686

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272364T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406647T>C , CM000666.2:g.73406647T>C	GRCh38
NC_000004.11:g.74272364T>C , CM000666.1:g.74272364T>C	GRCh37
NC_000004.10:g.74491228T>C	NCBI36
NG_009291.1:g.7393T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.156T>C MANE Select	ENSP00000295897.4:p.Ala52=
ENST00000295897.8:c.156T>C	ENSP00000295897.4:p.Ala52=
ENST00000401494.7:c.137+1474T>C	ENSP00000384695.3:n.137+1474T>C
ENST00000415165.6:c.137+1474T>C	ENSP00000401820.2:n.137+1474T>C
ENST00000441319.5:c.162T>C	ENSP00000392541.1:p.Ala54=
ENST00000476441.6:c.79+2241T>C	ENSP00000423727.1:n.79+2241T>C
ENST00000503124.5:c.-83T>C	ENSP00000421027.1:n.-83T>C
ENST00000509063.5:c.156T>C	ENSP00000422784.1:p.Ala52=
ENST00000510166.5:n.192T>C
ENST00000514786.1:n.125T>C
ENST00000515133.5:n.197T>C
ENST00000621085.4:c.156T>C	ENSP00000483421.1:p.Ala52=
ENST00000621628.4:c.156T>C	ENSP00000480485.1:p.Ala52=
NM_000477.5:c.156T>C	NP_000468.1:p.Ala52=
NM_000477.6:c.156T>C	NP_000468.1:p.Ala52=
NM_000477.7:c.156T>C MANE Select	NP_000468.1:p.Ala52=