Canonical Allele Identifier: CA1468148137

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419530A= , CM000666.2:g.73419530A=	GRCh38
NC_000004.11:g.74285247A= , CM000666.1:g.74285247A=	GRCh37
NC_000004.10:g.74504111A=	NCBI36
NG_009291.1:g.20276A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1676A= MANE Select	ENSP00000295897.4:p.His559=
ENST00000295897.8:c.1676A=	ENSP00000295897.4:p.His559=
ENST00000401494.7:c.1331A=	ENSP00000384695.3:p.His444=
ENST00000415165.6:c.1100A=	ENSP00000401820.2:p.His367=
ENST00000476441.6:c.*955A=	ENSP00000423727.1:n.*955A=
ENST00000486939.1:n.330A=
ENST00000503124.5:c.1226A=	ENSP00000421027.1:p.His409=
ENST00000505649.5:n.1223A=
ENST00000508932.5:n.175+75A=
ENST00000509063.5:c.1676A=	ENSP00000422784.1:p.His559=
ENST00000511370.1:c.1209A=
ENST00000621085.4:c.1037A=	ENSP00000483421.1:p.His346=
ENST00000621628.4:c.1037A=	ENSP00000480485.1:p.His346=
NM_000477.5:c.1676A=	NP_000468.1:p.His559=
NM_000477.6:c.1676A=	NP_000468.1:p.His559=
NM_000477.7:c.1676A= MANE Select	NP_000468.1:p.His559=