Canonical Allele Identifier: CA439800307

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280812T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415095T>C , CM000666.2:g.73415095T>C	GRCh38
NC_000004.11:g.74280812T>C , CM000666.1:g.74280812T>C	GRCh37
NC_000004.10:g.74499676T>C	NCBI36
NG_009291.1:g.15841T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1119T>C MANE Select	ENSP00000295897.4:p.Leu373=
ENST00000295897.8:c.1119T>C	ENSP00000295897.4:p.Leu373=
ENST00000401494.7:c.774T>C	ENSP00000384695.3:p.Leu258=
ENST00000415165.6:c.543T>C	ENSP00000401820.2:p.Leu181=
ENST00000476441.6:c.*398T>C	ENSP00000423727.1:n.*398T>C
ENST00000484992.1:n.439T>C
ENST00000503124.5:c.669T>C	ENSP00000421027.1:p.Leu223=
ENST00000504043.1:n.122T>C
ENST00000505649.5:n.805T>C
ENST00000509063.5:c.1119T>C	ENSP00000422784.1:p.Leu373=
ENST00000511370.1:c.652T>C
ENST00000621085.4:c.491-11T>C	ENSP00000483421.1:n.491-11T>C
ENST00000621628.4:c.487-7T>C	ENSP00000480485.1:n.487-7T>C
NM_000477.5:c.1119T>C	NP_000468.1:p.Leu373=
NM_000477.6:c.1119T>C	NP_000468.1:p.Leu373=
NM_000477.7:c.1119T>C MANE Select	NP_000468.1:p.Leu373=