Canonical Allele Identifier: CA357241154

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280789T>A (hg19) ; chr4:g.73415072T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415072T>A , CM000666.2:g.73415072T>A	GRCh38
NC_000004.11:g.74280789T>A , CM000666.1:g.74280789T>A	GRCh37
NC_000004.10:g.74499653T>A	NCBI36
NG_009291.1:g.15818T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1096T>A MANE Select	ENSP00000295897.4:p.Ser366Thr
ENST00000295897.8:c.1096T>A	ENSP00000295897.4:p.Ser366Thr
ENST00000401494.7:c.751T>A	ENSP00000384695.3:p.Ser251Thr
ENST00000415165.6:c.520T>A	ENSP00000401820.2:p.Ser174Thr
ENST00000476441.6:c.*375T>A	ENSP00000423727.1:n.*375T>A
ENST00000484992.1:n.416T>A
ENST00000503124.5:c.646T>A	ENSP00000421027.1:p.Ser216Thr
ENST00000504043.1:n.99T>A
ENST00000505649.5:n.782T>A
ENST00000509063.5:c.1096T>A	ENSP00000422784.1:p.Ser366Thr
ENST00000511370.1:c.629T>A
ENST00000621085.4:c.491-34T>A	ENSP00000483421.1:n.491-34T>A
ENST00000621628.4:c.487-30T>A	ENSP00000480485.1:n.487-30T>A
NM_000477.5:c.1096T>A	NP_000468.1:p.Ser366Thr
NM_000477.6:c.1096T>A	NP_000468.1:p.Ser366Thr
NM_000477.7:c.1096T>A MANE Select	NP_000468.1:p.Ser366Thr