Canonical Allele Identifier: CA357238387

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275199C>A (hg19) ; chr4:g.73409482C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409482C>A , CM000666.2:g.73409482C>A	GRCh38
NC_000004.11:g.74275199C>A , CM000666.1:g.74275199C>A	GRCh37
NC_000004.10:g.74494063C>A	NCBI36
NG_009291.1:g.10228C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.610C>A MANE Select	ENSP00000295897.4:p.Pro204Thr
ENST00000295897.8:c.610C>A	ENSP00000295897.4:p.Pro204Thr
ENST00000401494.7:c.265C>A	ENSP00000384695.3:p.Pro89Thr
ENST00000415165.6:c.138-2514C>A	ENSP00000401820.2:n.138-2514C>A
ENST00000476441.6:c.207C>A	ENSP00000423727.1:p.Cys69Ter
ENST00000503124.5:c.160C>A	ENSP00000421027.1:p.Pro54Thr
ENST00000505649.5:n.296C>A
ENST00000509063.5:c.610C>A	ENSP00000422784.1:p.Pro204Thr
ENST00000511370.1:c.143C>A
ENST00000621085.4:c.490+120C>A	ENSP00000483421.1:n.490+120C>A
ENST00000621628.4:c.486+406C>A	ENSP00000480485.1:n.486+406C>A
NM_000477.5:c.610C>A	NP_000468.1:p.Pro204Thr
NM_000477.6:c.610C>A	NP_000468.1:p.Pro204Thr
NM_000477.7:c.610C>A MANE Select	NP_000468.1:p.Pro204Thr