Canonical Allele Identifier: CA357238089

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275103T>G (hg19) ; chr4:g.73409386T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409386T>G , CM000666.2:g.73409386T>G	GRCh38
NC_000004.11:g.74275103T>G , CM000666.1:g.74275103T>G	GRCh37
NC_000004.10:g.74493967T>G	NCBI36
NG_009291.1:g.10132T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.514T>G MANE Select	ENSP00000295897.4:p.Tyr172Asp
ENST00000295897.8:c.514T>G	ENSP00000295897.4:p.Tyr172Asp
ENST00000401494.7:c.169T>G	ENSP00000384695.3:p.Tyr57Asp
ENST00000415165.6:c.138-2610T>G	ENSP00000401820.2:n.138-2610T>G
ENST00000441319.5:c.520T>G	ENSP00000392541.1:p.Tyr174Asp
ENST00000476441.6:c.111T>G	ENSP00000423727.1:p.Leu37=
ENST00000503124.5:c.64T>G	ENSP00000421027.1:p.Tyr22Asp
ENST00000505649.5:n.200T>G
ENST00000509063.5:c.514T>G	ENSP00000422784.1:p.Tyr172Asp
ENST00000511370.1:c.47T>G
ENST00000514786.1:n.483T>G
ENST00000621085.4:c.490+24T>G	ENSP00000483421.1:n.490+24T>G
ENST00000621628.4:c.486+310T>G	ENSP00000480485.1:n.486+310T>G
NM_000477.5:c.514T>G	NP_000468.1:p.Tyr172Asp
NM_000477.6:c.514T>G	NP_000468.1:p.Tyr172Asp
NM_000477.7:c.514T>G MANE Select	NP_000468.1:p.Tyr172Asp