Canonical Allele Identifier: CA1468152497

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409034A= , CM000666.2:g.73409034A=	GRCh38
NC_000004.11:g.74274751A= , CM000666.1:g.74274751A=	GRCh37
NC_000004.10:g.74493615A=	NCBI36
NG_009291.1:g.9780A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+229A= MANE Select	ENSP00000295897.4:n.482+229A=
ENST00000295897.8:c.482+229A=	ENSP00000295897.4:n.482+229A=
ENST00000401494.7:c.138-321A=	ENSP00000384695.3:n.138-321A=
ENST00000415165.6:c.138-2962A=	ENSP00000401820.2:n.138-2962A=
ENST00000441319.5:c.488+229A=	ENSP00000392541.1:n.488+229A=
ENST00000476441.6:c.80-321A=	ENSP00000423727.1:n.80-321A=
ENST00000503124.5:c.33-321A=	ENSP00000421027.1:n.33-321A=
ENST00000505649.5:n.168+229A=
ENST00000509063.5:c.482+229A=	ENSP00000422784.1:n.482+229A=
ENST00000514786.1:n.451+229A=
ENST00000621085.4:c.482+229A=	ENSP00000483421.1:n.482+229A=
ENST00000621628.4:c.483-39A=	ENSP00000480485.1:n.483-39A=
NM_000477.5:c.482+229A=	NP_000468.1:n.482+229A=
NM_000477.6:c.482+229A=	NP_000468.1:n.482+229A=
NM_000477.7:c.482+229A= MANE Select	NP_000468.1:n.482+229A=