Canonical Allele Identifier: CA439800910

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285275G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419558G>C , CM000666.2:g.73419558G>C	GRCh38
NC_000004.11:g.74285275G>C , CM000666.1:g.74285275G>C	GRCh37
NC_000004.10:g.74504139G>C	NCBI36
NG_009291.1:g.20304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1704G>C MANE Select	ENSP00000295897.4:p.Leu568=
ENST00000295897.8:c.1704G>C	ENSP00000295897.4:p.Leu568=
ENST00000401494.7:c.1359G>C	ENSP00000384695.3:p.Leu453=
ENST00000415165.6:c.1128G>C	ENSP00000401820.2:p.Leu376=
ENST00000476441.6:c.*983G>C	ENSP00000423727.1:n.*983G>C
ENST00000495173.1:n.12G>C
ENST00000503124.5:c.1254G>C	ENSP00000421027.1:p.Leu418=
ENST00000505649.5:n.1251G>C
ENST00000508932.5:n.175+103G>C
ENST00000509063.5:c.1704G>C	ENSP00000422784.1:p.Leu568=
ENST00000511370.1:c.1237G>C
ENST00000621085.4:c.1065G>C	ENSP00000483421.1:p.Leu355=
ENST00000621628.4:c.1065G>C	ENSP00000480485.1:p.Leu355=
NM_000477.5:c.1704G>C	NP_000468.1:p.Leu568=
NM_000477.6:c.1704G>C	NP_000468.1:p.Leu568=
NM_000477.7:c.1704G>C MANE Select	NP_000468.1:p.Leu568=