Canonical Allele Identifier: CA439799418

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275102T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409385T>A , CM000666.2:g.73409385T>A	GRCh38
NC_000004.11:g.74275102T>A , CM000666.1:g.74275102T>A	GRCh37
NC_000004.10:g.74493966T>A	NCBI36
NG_009291.1:g.10131T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.513T>A MANE Select	ENSP00000295897.4:p.Pro171=
ENST00000295897.8:c.513T>A	ENSP00000295897.4:p.Pro171=
ENST00000401494.7:c.168T>A	ENSP00000384695.3:p.Pro56=
ENST00000415165.6:c.138-2611T>A	ENSP00000401820.2:n.138-2611T>A
ENST00000441319.5:c.519T>A	ENSP00000392541.1:p.Pro173=
ENST00000476441.6:c.110T>A	ENSP00000423727.1:p.Leu37His
ENST00000503124.5:c.63T>A	ENSP00000421027.1:p.Pro21=
ENST00000505649.5:n.199T>A
ENST00000509063.5:c.513T>A	ENSP00000422784.1:p.Pro171=
ENST00000511370.1:c.46T>A
ENST00000514786.1:n.482T>A
ENST00000621085.4:c.490+23T>A	ENSP00000483421.1:n.490+23T>A
ENST00000621628.4:c.486+309T>A	ENSP00000480485.1:n.486+309T>A
NM_000477.5:c.513T>A	NP_000468.1:p.Pro171=
NM_000477.6:c.513T>A	NP_000468.1:p.Pro171=
NM_000477.7:c.513T>A MANE Select	NP_000468.1:p.Pro171=