Canonical Allele Identifier: CA1468152675

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409384C= , CM000666.2:g.73409384C=	GRCh38
NC_000004.11:g.74275101C= , CM000666.1:g.74275101C=	GRCh37
NC_000004.10:g.74493965C=	NCBI36
NG_009291.1:g.10130C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.512C= MANE Select	ENSP00000295897.4:p.Pro171=
ENST00000295897.8:c.512C=	ENSP00000295897.4:p.Pro171=
ENST00000401494.7:c.167C=	ENSP00000384695.3:p.Pro56=
ENST00000415165.6:c.138-2612C=	ENSP00000401820.2:n.138-2612C=
ENST00000441319.5:c.518C=	ENSP00000392541.1:p.Pro173=
ENST00000476441.6:c.109C=	ENSP00000423727.1:p.Leu37=
ENST00000503124.5:c.62C=	ENSP00000421027.1:p.Pro21=
ENST00000505649.5:n.198C=
ENST00000509063.5:c.512C=	ENSP00000422784.1:p.Pro171=
ENST00000511370.1:c.45C=
ENST00000514786.1:n.481C=
ENST00000621085.4:c.490+22C=	ENSP00000483421.1:n.490+22C=
ENST00000621628.4:c.486+308C=	ENSP00000480485.1:n.486+308C=
NM_000477.5:c.512C=	NP_000468.1:p.Pro171=
NM_000477.6:c.512C=	NP_000468.1:p.Pro171=
NM_000477.7:c.512C= MANE Select	NP_000468.1:p.Pro171=