Canonical Allele Identifier: CA439799407

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275091A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409374A>C , CM000666.2:g.73409374A>C	GRCh38
NC_000004.11:g.74275091A>C , CM000666.1:g.74275091A>C	GRCh37
NC_000004.10:g.74493955A>C	NCBI36
NG_009291.1:g.10120A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.502A>C MANE Select	ENSP00000295897.4:p.Arg168=
ENST00000295897.8:c.502A>C	ENSP00000295897.4:p.Arg168=
ENST00000401494.7:c.157A>C	ENSP00000384695.3:p.Arg53=
ENST00000415165.6:c.138-2622A>C	ENSP00000401820.2:n.138-2622A>C
ENST00000441319.5:c.508A>C	ENSP00000392541.1:p.Arg170=
ENST00000476441.6:c.99A>C	ENSP00000423727.1:p.Pro33=
ENST00000503124.5:c.52A>C	ENSP00000421027.1:p.Arg18=
ENST00000505649.5:n.188A>C
ENST00000509063.5:c.502A>C	ENSP00000422784.1:p.Arg168=
ENST00000511370.1:c.35A>C
ENST00000514786.1:n.471A>C
ENST00000621085.4:c.490+12A>C	ENSP00000483421.1:n.490+12A>C
ENST00000621628.4:c.486+298A>C	ENSP00000480485.1:n.486+298A>C
NM_000477.5:c.502A>C	NP_000468.1:p.Arg168=
NM_000477.6:c.502A>C	NP_000468.1:p.Arg168=
NM_000477.7:c.502A>C MANE Select	NP_000468.1:p.Arg168=