Canonical Allele Identifier: CA357238166

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275137A>C (hg19) ; chr4:g.73409420A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409420A>C , CM000666.2:g.73409420A>C	GRCh38
NC_000004.11:g.74275137A>C , CM000666.1:g.74275137A>C	GRCh37
NC_000004.10:g.74494001A>C	NCBI36
NG_009291.1:g.10166A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.548A>C MANE Select	ENSP00000295897.4:p.Lys183Thr
ENST00000295897.8:c.548A>C	ENSP00000295897.4:p.Lys183Thr
ENST00000401494.7:c.203A>C	ENSP00000384695.3:p.Lys68Thr
ENST00000415165.6:c.138-2576A>C	ENSP00000401820.2:n.138-2576A>C
ENST00000441319.5:c.554A>C	ENSP00000392541.1:p.Lys185Thr
ENST00000476441.6:c.145A>C	ENSP00000423727.1:p.Lys49Gln
ENST00000503124.5:c.98A>C	ENSP00000421027.1:p.Lys33Thr
ENST00000505649.5:n.234A>C
ENST00000509063.5:c.548A>C	ENSP00000422784.1:p.Lys183Thr
ENST00000511370.1:c.81A>C
ENST00000514786.1:n.517A>C
ENST00000621085.4:c.490+58A>C	ENSP00000483421.1:n.490+58A>C
ENST00000621628.4:c.486+344A>C	ENSP00000480485.1:n.486+344A>C
NM_000477.5:c.548A>C	NP_000468.1:p.Lys183Thr
NM_000477.6:c.548A>C	NP_000468.1:p.Lys183Thr
NM_000477.7:c.548A>C MANE Select	NP_000468.1:p.Lys183Thr