Canonical Allele Identifier: CA1468152674

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409381A= , CM000666.2:g.73409381A=	GRCh38
NC_000004.11:g.74275098A= , CM000666.1:g.74275098A=	GRCh37
NC_000004.10:g.74493962A=	NCBI36
NG_009291.1:g.10127A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.509A= MANE Select	ENSP00000295897.4:p.His170=
ENST00000295897.8:c.509A=	ENSP00000295897.4:p.His170=
ENST00000401494.7:c.164A=	ENSP00000384695.3:p.His55=
ENST00000415165.6:c.138-2615A=	ENSP00000401820.2:n.138-2615A=
ENST00000441319.5:c.515A=	ENSP00000392541.1:p.His172=
ENST00000476441.6:c.106A=	ENSP00000423727.1:p.Ile36=
ENST00000503124.5:c.59A=	ENSP00000421027.1:p.His20=
ENST00000505649.5:n.195A=
ENST00000509063.5:c.509A=	ENSP00000422784.1:p.His170=
ENST00000511370.1:c.42A=
ENST00000514786.1:n.478A=
ENST00000621085.4:c.490+19A=	ENSP00000483421.1:n.490+19A=
ENST00000621628.4:c.486+305A=	ENSP00000480485.1:n.486+305A=
NM_000477.5:c.509A=	NP_000468.1:p.His170=
NM_000477.6:c.509A=	NP_000468.1:p.His170=
NM_000477.7:c.509A= MANE Select	NP_000468.1:p.His170=