Canonical Allele Identifier: CA357239060

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74277718T>G (hg19) ; chr4:g.73412001T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73412001T>G , CM000666.2:g.73412001T>G	GRCh38
NC_000004.11:g.74277718T>G , CM000666.1:g.74277718T>G	GRCh37
NC_000004.10:g.74496582T>G	NCBI36
NG_009291.1:g.12747T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.719T>G MANE Select	ENSP00000295897.4:p.Val240Gly
ENST00000295897.8:c.719T>G	ENSP00000295897.4:p.Val240Gly
ENST00000401494.7:c.374T>G	ENSP00000384695.3:p.Val125Gly
ENST00000415165.6:c.143T>G	ENSP00000401820.2:p.Val48Gly
ENST00000476441.6:c.316T>G	ENSP00000423727.1:p.Ter106Glu
ENST00000503124.5:c.269T>G	ENSP00000421027.1:p.Val90Gly
ENST00000505649.5:n.405T>G
ENST00000507673.1:n.36T>G
ENST00000509063.5:c.719T>G	ENSP00000422784.1:p.Val240Gly
ENST00000511370.1:c.252T>G
ENST00000621085.4:c.490+2639T>G	ENSP00000483421.1:n.490+2639T>G
ENST00000621628.4:c.486+2925T>G	ENSP00000480485.1:n.486+2925T>G
NM_000477.5:c.719T>G	NP_000468.1:p.Val240Gly
NM_000477.6:c.719T>G	NP_000468.1:p.Val240Gly
NM_000477.7:c.719T>G MANE Select	NP_000468.1:p.Val240Gly