Canonical Allele Identifier: CA357247270

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286007G>C (hg19) ; chr4:g.73420290G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420290G>C , CM000666.2:g.73420290G>C	GRCh38
NC_000004.11:g.74286007G>C , CM000666.1:g.74286007G>C	GRCh37
NC_000004.10:g.74504871G>C	NCBI36
NG_009291.1:g.21036G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1822G>C MANE Select	ENSP00000295897.4:p.Gly608Arg
ENST00000295897.8:c.1822G>C	ENSP00000295897.4:p.Gly608Arg
ENST00000401494.7:c.1477G>C	ENSP00000384695.3:p.Gly493Arg
ENST00000415165.6:c.1246G>C	ENSP00000401820.2:p.Gly416Arg
ENST00000476441.6:c.*1101G>C	ENSP00000423727.1:n.*1101G>C
ENST00000495173.1:n.130G>C
ENST00000503124.5:c.1372G>C	ENSP00000421027.1:p.Gly458Arg
ENST00000505649.5:n.1369G>C
ENST00000508932.5:n.212G>C
ENST00000509063.5:c.1785+651G>C	ENSP00000422784.1:n.1785+651G>C
ENST00000511370.1:c.1355G>C
ENST00000621085.4:c.1183G>C	ENSP00000483421.1:p.Gly395Arg
ENST00000621628.4:c.1183G>C	ENSP00000480485.1:p.Gly395Arg
NM_000477.5:c.1822G>C	NP_000468.1:p.Gly608Arg
NM_000477.6:c.1822G>C	NP_000468.1:p.Gly608Arg
NM_000477.7:c.1822G>C MANE Select	NP_000468.1:p.Gly608Arg