Canonical Allele Identifier: CA1468143678

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415173T= , CM000666.2:g.73415173T=	GRCh38
NC_000004.11:g.74280890T= , CM000666.1:g.74280890T=	GRCh37
NC_000004.10:g.74499754T=	NCBI36
NG_009291.1:g.15919T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+6T= MANE Select	ENSP00000295897.4:n.1191+6T=
ENST00000295897.8:c.1191+6T=	ENSP00000295897.4:n.1191+6T=
ENST00000401494.7:c.846+6T=	ENSP00000384695.3:n.846+6T=
ENST00000415165.6:c.615+6T=	ENSP00000401820.2:n.615+6T=
ENST00000476441.6:c.*470+6T=	ENSP00000423727.1:n.*470+6T=
ENST00000484992.1:n.511+6T=
ENST00000503124.5:c.741+6T=	ENSP00000421027.1:n.741+6T=
ENST00000504043.1:n.200T=
ENST00000505649.5:n.877+6T=
ENST00000509063.5:c.1191+6T=	ENSP00000422784.1:n.1191+6T=
ENST00000511370.1:c.724+6T=
ENST00000621085.4:c.552+6T=	ENSP00000483421.1:n.552+6T=
ENST00000621628.4:c.552+6T=	ENSP00000480485.1:n.552+6T=
NM_000477.5:c.1191+6T=	NP_000468.1:n.1191+6T=
NM_000477.6:c.1191+6T=	NP_000468.1:n.1191+6T=
NM_000477.7:c.1191+6T= MANE Select	NP_000468.1:n.1191+6T=