Canonical Allele Identifier: CA439800252

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280756T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415039T>C , CM000666.2:g.73415039T>C	GRCh38
NC_000004.11:g.74280756T>C , CM000666.1:g.74280756T>C	GRCh37
NC_000004.10:g.74499620T>C	NCBI36
NG_009291.1:g.15785T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1063T>C MANE Select	ENSP00000295897.4:p.Leu355=
ENST00000295897.8:c.1063T>C	ENSP00000295897.4:p.Leu355=
ENST00000401494.7:c.718T>C	ENSP00000384695.3:p.Leu240=
ENST00000415165.6:c.487T>C	ENSP00000401820.2:p.Leu163=
ENST00000476441.6:c.*342T>C	ENSP00000423727.1:n.*342T>C
ENST00000484992.1:n.383T>C
ENST00000503124.5:c.613T>C	ENSP00000421027.1:p.Leu205=
ENST00000504043.1:n.66T>C
ENST00000505649.5:n.749T>C
ENST00000509063.5:c.1063T>C	ENSP00000422784.1:p.Leu355=
ENST00000511370.1:c.596T>C
ENST00000621085.4:c.491-67T>C	ENSP00000483421.1:n.491-67T>C
ENST00000621628.4:c.487-63T>C	ENSP00000480485.1:n.487-63T>C
NM_000477.5:c.1063T>C	NP_000468.1:p.Leu355=
NM_000477.6:c.1063T>C	NP_000468.1:p.Leu355=
NM_000477.7:c.1063T>C MANE Select	NP_000468.1:p.Leu355=