Canonical Allele Identifier: CA357240579

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279186A>C (hg19) ; chr4:g.73413469A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413469A>C , CM000666.2:g.73413469A>C	GRCh38
NC_000004.11:g.74279186A>C , CM000666.1:g.74279186A>C	GRCh37
NC_000004.10:g.74498050A>C	NCBI36
NG_009291.1:g.14215A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.893A>C MANE Select	ENSP00000295897.4:p.Lys298Thr
ENST00000295897.8:c.893A>C	ENSP00000295897.4:p.Lys298Thr
ENST00000401494.7:c.548A>C	ENSP00000384695.3:p.Lys183Thr
ENST00000415165.6:c.317A>C	ENSP00000401820.2:p.Lys106Thr
ENST00000476441.6:c.*172A>C	ENSP00000423727.1:n.*172A>C
ENST00000484992.1:n.213A>C
ENST00000503124.5:c.443A>C	ENSP00000421027.1:p.Lys148Thr
ENST00000505649.5:n.579A>C
ENST00000509063.5:c.893A>C	ENSP00000422784.1:p.Lys298Thr
ENST00000511370.1:c.426A>C
ENST00000621085.4:c.491-1637A>C	ENSP00000483421.1:n.491-1637A>C
ENST00000621628.4:c.487-1633A>C	ENSP00000480485.1:n.487-1633A>C
NM_000477.5:c.893A>C	NP_000468.1:p.Lys298Thr
NM_000477.6:c.893A>C	NP_000468.1:p.Lys298Thr
NM_000477.7:c.893A>C MANE Select	NP_000468.1:p.Lys298Thr