Canonical Allele Identifier: CA357240507

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279168A>C (hg19) ; chr4:g.73413451A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413451A>C , CM000666.2:g.73413451A>C	GRCh38
NC_000004.11:g.74279168A>C , CM000666.1:g.74279168A>C	GRCh37
NC_000004.10:g.74498032A>C	NCBI36
NG_009291.1:g.14197A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.875A>C MANE Select	ENSP00000295897.4:p.Gln292Pro
ENST00000295897.8:c.875A>C	ENSP00000295897.4:p.Gln292Pro
ENST00000401494.7:c.530A>C	ENSP00000384695.3:p.Gln177Pro
ENST00000415165.6:c.299A>C	ENSP00000401820.2:p.Gln100Pro
ENST00000476441.6:c.*154A>C	ENSP00000423727.1:n.*154A>C
ENST00000484992.1:n.195A>C
ENST00000503124.5:c.425A>C	ENSP00000421027.1:p.Gln142Pro
ENST00000505649.5:n.561A>C
ENST00000509063.5:c.875A>C	ENSP00000422784.1:p.Gln292Pro
ENST00000511370.1:c.408A>C
ENST00000621085.4:c.491-1655A>C	ENSP00000483421.1:n.491-1655A>C
ENST00000621628.4:c.487-1651A>C	ENSP00000480485.1:n.487-1651A>C
NM_000477.5:c.875A>C	NP_000468.1:p.Gln292Pro
NM_000477.6:c.875A>C	NP_000468.1:p.Gln292Pro
NM_000477.7:c.875A>C MANE Select	NP_000468.1:p.Gln292Pro