Canonical Allele Identifier: CA357246316

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285288G>C (hg19) ; chr4:g.73419571G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419571G>C , CM000666.2:g.73419571G>C	GRCh38
NC_000004.11:g.74285288G>C , CM000666.1:g.74285288G>C	GRCh37
NC_000004.10:g.74504152G>C	NCBI36
NG_009291.1:g.20317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1717G>C MANE Select	ENSP00000295897.4:p.Asp573His
ENST00000295897.8:c.1717G>C	ENSP00000295897.4:p.Asp573His
ENST00000401494.7:c.1372G>C	ENSP00000384695.3:p.Asp458His
ENST00000415165.6:c.1141G>C	ENSP00000401820.2:p.Asp381His
ENST00000476441.6:c.*996G>C	ENSP00000423727.1:n.*996G>C
ENST00000495173.1:n.25G>C
ENST00000503124.5:c.1267G>C	ENSP00000421027.1:p.Asp423His
ENST00000505649.5:n.1264G>C
ENST00000508932.5:n.175+116G>C
ENST00000509063.5:c.1717G>C	ENSP00000422784.1:p.Asp573His
ENST00000511370.1:c.1250G>C
ENST00000621085.4:c.1078G>C	ENSP00000483421.1:p.Asp360His
ENST00000621628.4:c.1078G>C	ENSP00000480485.1:p.Asp360His
NM_000477.5:c.1717G>C	NP_000468.1:p.Asp573His
NM_000477.6:c.1717G>C	NP_000468.1:p.Asp573His
NM_000477.7:c.1717G>C MANE Select	NP_000468.1:p.Asp573His