Canonical Allele Identifier: CA357246695

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285344C>A (hg19) ; chr4:g.73419627C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419627C>A , CM000666.2:g.73419627C>A	GRCh38
NC_000004.11:g.74285344C>A , CM000666.1:g.74285344C>A	GRCh37
NC_000004.10:g.74504208C>A	NCBI36
NG_009291.1:g.20373C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1773C>A MANE Select	ENSP00000295897.4:p.Cys591Ter
ENST00000295897.8:c.1773C>A	ENSP00000295897.4:p.Cys591Ter
ENST00000401494.7:c.1428C>A	ENSP00000384695.3:p.Cys476Ter
ENST00000415165.6:c.1197C>A	ENSP00000401820.2:p.Cys399Ter
ENST00000476441.6:c.*1052C>A	ENSP00000423727.1:n.*1052C>A
ENST00000495173.1:n.81C>A
ENST00000503124.5:c.1323C>A	ENSP00000421027.1:p.Cys441Ter
ENST00000505649.5:n.1320C>A
ENST00000508932.5:n.175+172C>A
ENST00000509063.5:c.1773C>A	ENSP00000422784.1:p.Cys591Ter
ENST00000511370.1:c.1306C>A
ENST00000621085.4:c.1134C>A	ENSP00000483421.1:p.Cys378Ter
ENST00000621628.4:c.1134C>A	ENSP00000480485.1:p.Cys378Ter
NM_000477.5:c.1773C>A	NP_000468.1:p.Cys591Ter
NM_000477.6:c.1773C>A	NP_000468.1:p.Cys591Ter
NM_000477.7:c.1773C>A MANE Select	NP_000468.1:p.Cys591Ter