Canonical Allele Identifier: CA1468152753

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409534T= , CM000666.2:g.73409534T=	GRCh38
NC_000004.11:g.74275251T= , CM000666.1:g.74275251T=	GRCh37
NC_000004.10:g.74494115T=	NCBI36
NG_009291.1:g.10280T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.615+47T= MANE Select	ENSP00000295897.4:n.615+47T=
ENST00000295897.8:c.615+47T=	ENSP00000295897.4:n.615+47T=
ENST00000401494.7:c.270+47T=	ENSP00000384695.3:n.270+47T=
ENST00000415165.6:c.138-2462T=	ENSP00000401820.2:n.138-2462T=
ENST00000476441.6:c.212+47T=	ENSP00000423727.1:n.212+47T=
ENST00000503124.5:c.165+47T=	ENSP00000421027.1:n.165+47T=
ENST00000505649.5:n.301+47T=
ENST00000509063.5:c.615+47T=	ENSP00000422784.1:n.615+47T=
ENST00000511370.1:c.148+47T=
ENST00000621085.4:c.490+172T=	ENSP00000483421.1:n.490+172T=
ENST00000621628.4:c.486+458T=	ENSP00000480485.1:n.486+458T=
NM_000477.5:c.615+47T=	NP_000468.1:n.615+47T=
NM_000477.6:c.615+47T=	NP_000468.1:n.615+47T=
NM_000477.7:c.615+47T= MANE Select	NP_000468.1:n.615+47T=