Canonical Allele Identifier: CA357246675

Gene: ALB

Linked Data

• gnomAD v4: 4-73419625-T-C
• MyVariant Identifiers: chr4:g.74285342T>C (hg19) ; chr4:g.73419625T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419625T>C , CM000666.2:g.73419625T>C	GRCh38
NC_000004.11:g.74285342T>C , CM000666.1:g.74285342T>C	GRCh37
NC_000004.10:g.74504206T>C	NCBI36
NG_009291.1:g.20371T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1771T>C MANE Select	ENSP00000295897.4:p.Cys591Arg
ENST00000295897.8:c.1771T>C	ENSP00000295897.4:p.Cys591Arg
ENST00000401494.7:c.1426T>C	ENSP00000384695.3:p.Cys476Arg
ENST00000415165.6:c.1195T>C	ENSP00000401820.2:p.Cys399Arg
ENST00000476441.6:c.*1050T>C	ENSP00000423727.1:n.*1050T>C
ENST00000495173.1:n.79T>C
ENST00000503124.5:c.1321T>C	ENSP00000421027.1:p.Cys441Arg
ENST00000505649.5:n.1318T>C
ENST00000508932.5:n.175+170T>C
ENST00000509063.5:c.1771T>C	ENSP00000422784.1:p.Cys591Arg
ENST00000511370.1:c.1304T>C
ENST00000621085.4:c.1132T>C	ENSP00000483421.1:p.Cys378Arg
ENST00000621628.4:c.1132T>C	ENSP00000480485.1:p.Cys378Arg
NM_000477.5:c.1771T>C	NP_000468.1:p.Cys591Arg
NM_000477.6:c.1771T>C	NP_000468.1:p.Cys591Arg
NM_000477.7:c.1771T>C MANE Select	NP_000468.1:p.Cys591Arg