Canonical Allele Identifier: CA439801012

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285347T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419630T>C , CM000666.2:g.73419630T>C	GRCh38
NC_000004.11:g.74285347T>C , CM000666.1:g.74285347T>C	GRCh37
NC_000004.10:g.74504211T>C	NCBI36
NG_009291.1:g.20376T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1776T>C MANE Select	ENSP00000295897.4:p.Phe592=
ENST00000295897.8:c.1776T>C	ENSP00000295897.4:p.Phe592=
ENST00000401494.7:c.1431T>C	ENSP00000384695.3:p.Phe477=
ENST00000415165.6:c.1200T>C	ENSP00000401820.2:p.Phe400=
ENST00000476441.6:c.*1055T>C	ENSP00000423727.1:n.*1055T>C
ENST00000495173.1:n.84T>C
ENST00000503124.5:c.1326T>C	ENSP00000421027.1:p.Phe442=
ENST00000505649.5:n.1323T>C
ENST00000508932.5:n.175+175T>C
ENST00000509063.5:c.1776T>C	ENSP00000422784.1:p.Phe592=
ENST00000511370.1:c.1309T>C
ENST00000621085.4:c.1137T>C	ENSP00000483421.1:p.Phe379=
ENST00000621628.4:c.1137T>C	ENSP00000480485.1:p.Phe379=
NM_000477.5:c.1776T>C	NP_000468.1:p.Phe592=
NM_000477.6:c.1776T>C	NP_000468.1:p.Phe592=
NM_000477.7:c.1776T>C MANE Select	NP_000468.1:p.Phe592=