Canonical Allele Identifier: CA357241445

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280852G>C (hg19) ; chr4:g.73415135G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415135G>C , CM000666.2:g.73415135G>C	GRCh38
NC_000004.11:g.74280852G>C , CM000666.1:g.74280852G>C	GRCh37
NC_000004.10:g.74499716G>C	NCBI36
NG_009291.1:g.15881G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1159G>C MANE Select	ENSP00000295897.4:p.Ala387Pro
ENST00000295897.8:c.1159G>C	ENSP00000295897.4:p.Ala387Pro
ENST00000401494.7:c.814G>C	ENSP00000384695.3:p.Ala272Pro
ENST00000415165.6:c.583G>C	ENSP00000401820.2:p.Ala195Pro
ENST00000476441.6:c.*438G>C	ENSP00000423727.1:n.*438G>C
ENST00000484992.1:n.479G>C
ENST00000503124.5:c.709G>C	ENSP00000421027.1:p.Ala237Pro
ENST00000504043.1:n.162G>C
ENST00000505649.5:n.845G>C
ENST00000509063.5:c.1159G>C	ENSP00000422784.1:p.Ala387Pro
ENST00000511370.1:c.692G>C
ENST00000621085.4:c.520G>C	ENSP00000483421.1:p.Ala174Pro
ENST00000621628.4:c.520G>C	ENSP00000480485.1:p.Ala174Pro
NM_000477.5:c.1159G>C	NP_000468.1:p.Ala387Pro
NM_000477.6:c.1159G>C	NP_000468.1:p.Ala387Pro
NM_000477.7:c.1159G>C MANE Select	NP_000468.1:p.Ala387Pro