Canonical Allele Identifier: CA357239045

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74277714G>C (hg19) ; chr4:g.73411997G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73411997G>C , CM000666.2:g.73411997G>C	GRCh38
NC_000004.11:g.74277714G>C , CM000666.1:g.74277714G>C	GRCh37
NC_000004.10:g.74496578G>C	NCBI36
NG_009291.1:g.12743G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.715G>C MANE Select	ENSP00000295897.4:p.Ala239Pro
ENST00000295897.8:c.715G>C	ENSP00000295897.4:p.Ala239Pro
ENST00000401494.7:c.370G>C	ENSP00000384695.3:p.Ala124Pro
ENST00000415165.6:c.139G>C	ENSP00000401820.2:p.Ala47Pro
ENST00000476441.6:c.312G>C	ENSP00000423727.1:p.Gly104=
ENST00000503124.5:c.265G>C	ENSP00000421027.1:p.Ala89Pro
ENST00000505649.5:n.401G>C
ENST00000507673.1:n.32G>C
ENST00000509063.5:c.715G>C	ENSP00000422784.1:p.Ala239Pro
ENST00000511370.1:c.248G>C
ENST00000621085.4:c.490+2635G>C	ENSP00000483421.1:n.490+2635G>C
ENST00000621628.4:c.486+2921G>C	ENSP00000480485.1:n.486+2921G>C
NM_000477.5:c.715G>C	NP_000468.1:p.Ala239Pro
NM_000477.6:c.715G>C	NP_000468.1:p.Ala239Pro
NM_000477.7:c.715G>C MANE Select	NP_000468.1:p.Ala239Pro