Canonical Allele Identifier: CA1468152725

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409486A= , CM000666.2:g.73409486A=	GRCh38
NC_000004.11:g.74275203A= , CM000666.1:g.74275203A=	GRCh37
NC_000004.10:g.74494067A=	NCBI36
NG_009291.1:g.10232A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.614A= MANE Select	ENSP00000295897.4:p.Lys205=
ENST00000295897.8:c.614A=	ENSP00000295897.4:p.Lys205=
ENST00000401494.7:c.269A=	ENSP00000384695.3:p.Lys90=
ENST00000415165.6:c.138-2510A=	ENSP00000401820.2:n.138-2510A=
ENST00000476441.6:c.211A=	ENSP00000423727.1:p.Ser71=
ENST00000503124.5:c.164A=	ENSP00000421027.1:p.Lys55=
ENST00000505649.5:n.300A=
ENST00000509063.5:c.614A=	ENSP00000422784.1:p.Lys205=
ENST00000511370.1:c.147A=
ENST00000621085.4:c.490+124A=	ENSP00000483421.1:n.490+124A=
ENST00000621628.4:c.486+410A=	ENSP00000480485.1:n.486+410A=
NM_000477.5:c.614A=	NP_000468.1:p.Lys205=
NM_000477.6:c.614A=	NP_000468.1:p.Lys205=
NM_000477.7:c.614A= MANE Select	NP_000468.1:p.Lys205=