Canonical Allele Identifier: CA357247125

Gene: ALB

Linked Data

• gnomAD v4: 4-73420269-G-A
• MyVariant Identifiers: chr4:g.74285986G>A (hg19) ; chr4:g.73420269G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420269G>A , CM000666.2:g.73420269G>A	GRCh38
NC_000004.11:g.74285986G>A , CM000666.1:g.74285986G>A	GRCh37
NC_000004.10:g.74504850G>A	NCBI36
NG_009291.1:g.21015G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1801G>A MANE Select	ENSP00000295897.4:p.Ala601Thr
ENST00000295897.8:c.1801G>A	ENSP00000295897.4:p.Ala601Thr
ENST00000401494.7:c.1456G>A	ENSP00000384695.3:p.Ala486Thr
ENST00000415165.6:c.1225G>A	ENSP00000401820.2:p.Ala409Thr
ENST00000476441.6:c.*1080G>A	ENSP00000423727.1:n.*1080G>A
ENST00000495173.1:n.109G>A
ENST00000503124.5:c.1351G>A	ENSP00000421027.1:p.Ala451Thr
ENST00000505649.5:n.1348G>A
ENST00000508932.5:n.191G>A
ENST00000509063.5:c.1785+630G>A	ENSP00000422784.1:n.1785+630G>A
ENST00000511370.1:c.1334G>A
ENST00000621085.4:c.1162G>A	ENSP00000483421.1:p.Ala388Thr
ENST00000621628.4:c.1162G>A	ENSP00000480485.1:p.Ala388Thr
NM_000477.5:c.1801G>A	NP_000468.1:p.Ala601Thr
NM_000477.6:c.1801G>A	NP_000468.1:p.Ala601Thr
NM_000477.7:c.1801G>A MANE Select	NP_000468.1:p.Ala601Thr