Canonical Allele Identifier: CA357238198

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275146A>C (hg19) ; chr4:g.73409429A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409429A>C , CM000666.2:g.73409429A>C	GRCh38
NC_000004.11:g.74275146A>C , CM000666.1:g.74275146A>C	GRCh37
NC_000004.10:g.74494010A>C	NCBI36
NG_009291.1:g.10175A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.557A>C MANE Select	ENSP00000295897.4:p.Lys186Thr
ENST00000295897.8:c.557A>C	ENSP00000295897.4:p.Lys186Thr
ENST00000401494.7:c.212A>C	ENSP00000384695.3:p.Lys71Thr
ENST00000415165.6:c.138-2567A>C	ENSP00000401820.2:n.138-2567A>C
ENST00000441319.5:c.563A>C	ENSP00000392541.1:p.Lys188Thr
ENST00000476441.6:c.154A>C	ENSP00000423727.1:p.Lys52Gln
ENST00000503124.5:c.107A>C	ENSP00000421027.1:p.Lys36Thr
ENST00000505649.5:n.243A>C
ENST00000509063.5:c.557A>C	ENSP00000422784.1:p.Lys186Thr
ENST00000511370.1:c.90A>C
ENST00000514786.1:n.526A>C
ENST00000621085.4:c.490+67A>C	ENSP00000483421.1:n.490+67A>C
ENST00000621628.4:c.486+353A>C	ENSP00000480485.1:n.486+353A>C
NM_000477.5:c.557A>C	NP_000468.1:p.Lys186Thr
NM_000477.6:c.557A>C	NP_000468.1:p.Lys186Thr
NM_000477.7:c.557A>C MANE Select	NP_000468.1:p.Lys186Thr