Canonical Allele Identifier: CA357244304

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283857G>T (hg19) ; chr4:g.73418140G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418140G>T , CM000666.2:g.73418140G>T	GRCh38
NC_000004.11:g.74283857G>T , CM000666.1:g.74283857G>T	GRCh37
NC_000004.10:g.74502721G>T	NCBI36
NG_009291.1:g.18886G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1481G>T MANE Select	ENSP00000295897.4:p.Ser494Ile
ENST00000295897.8:c.1481G>T	ENSP00000295897.4:p.Ser494Ile
ENST00000401494.7:c.1136G>T	ENSP00000384695.3:p.Ser379Ile
ENST00000415165.6:c.905G>T	ENSP00000401820.2:p.Ser302Ile
ENST00000476441.6:c.*760G>T	ENSP00000423727.1:n.*760G>T
ENST00000486939.1:n.135G>T
ENST00000503124.5:c.1031G>T	ENSP00000421027.1:p.Ser344Ile
ENST00000505649.5:n.1028G>T
ENST00000509063.5:c.1481G>T	ENSP00000422784.1:p.Ser494Ile
ENST00000511370.1:c.1014G>T
ENST00000621085.4:c.842G>T	ENSP00000483421.1:p.Ser281Ile
ENST00000621628.4:c.842G>T	ENSP00000480485.1:p.Ser281Ile
NM_000477.5:c.1481G>T	NP_000468.1:p.Ser494Ile
NM_000477.6:c.1481G>T	NP_000468.1:p.Ser494Ile
NM_000477.7:c.1481G>T MANE Select	NP_000468.1:p.Ser494Ile