Canonical Allele Identifier: CA1468152384

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408779T= , CM000666.2:g.73408779T=	GRCh38
NC_000004.11:g.74274496T= , CM000666.1:g.74274496T=	GRCh37
NC_000004.10:g.74493360T=	NCBI36
NG_009291.1:g.9525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.456T= MANE Select	ENSP00000295897.4:p.His152=
ENST00000295897.8:c.456T=	ENSP00000295897.4:p.His152=
ENST00000401494.7:c.138-576T=	ENSP00000384695.3:n.138-576T=
ENST00000415165.6:c.138-3217T=	ENSP00000401820.2:n.138-3217T=
ENST00000441319.5:c.462T=	ENSP00000392541.1:p.His154=
ENST00000476441.6:c.80-576T=	ENSP00000423727.1:n.80-576T=
ENST00000503124.5:c.33-576T=	ENSP00000421027.1:n.33-576T=
ENST00000505649.5:n.142T=
ENST00000509063.5:c.456T=	ENSP00000422784.1:p.His152=
ENST00000510166.5:n.492T=
ENST00000514786.1:n.425T=
ENST00000515133.5:n.497T=
ENST00000621085.4:c.456T=	ENSP00000483421.1:p.His152=
ENST00000621628.4:c.456T=	ENSP00000480485.1:p.His152=
NM_000477.5:c.456T=	NP_000468.1:p.His152=
NM_000477.6:c.456T=	NP_000468.1:p.His152=
NM_000477.7:c.456T= MANE Select	NP_000468.1:p.His152=