Canonical Allele Identifier: CA357247105

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285983G>T (hg19) ; chr4:g.73420266G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420266G>T , CM000666.2:g.73420266G>T	GRCh38
NC_000004.11:g.74285983G>T , CM000666.1:g.74285983G>T	GRCh37
NC_000004.10:g.74504847G>T	NCBI36
NG_009291.1:g.21012G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1798G>T MANE Select	ENSP00000295897.4:p.Val600Phe
ENST00000295897.8:c.1798G>T	ENSP00000295897.4:p.Val600Phe
ENST00000401494.7:c.1453G>T	ENSP00000384695.3:p.Val485Phe
ENST00000415165.6:c.1222G>T	ENSP00000401820.2:p.Val408Phe
ENST00000476441.6:c.*1077G>T	ENSP00000423727.1:n.*1077G>T
ENST00000495173.1:n.106G>T
ENST00000503124.5:c.1348G>T	ENSP00000421027.1:p.Val450Phe
ENST00000505649.5:n.1345G>T
ENST00000508932.5:n.188G>T
ENST00000509063.5:c.1785+627G>T	ENSP00000422784.1:n.1785+627G>T
ENST00000511370.1:c.1331G>T
ENST00000621085.4:c.1159G>T	ENSP00000483421.1:p.Val387Phe
ENST00000621628.4:c.1159G>T	ENSP00000480485.1:p.Val387Phe
NM_000477.5:c.1798G>T	NP_000468.1:p.Val600Phe
NM_000477.6:c.1798G>T	NP_000468.1:p.Val600Phe
NM_000477.7:c.1798G>T MANE Select	NP_000468.1:p.Val600Phe