Canonical Allele Identifier: CA357246085

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285243A>C (hg19) ; chr4:g.73419526A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419526A>C , CM000666.2:g.73419526A>C	GRCh38
NC_000004.11:g.74285243A>C , CM000666.1:g.74285243A>C	GRCh37
NC_000004.10:g.74504107A>C	NCBI36
NG_009291.1:g.20272A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1672A>C MANE Select	ENSP00000295897.4:p.Lys558Gln
ENST00000295897.8:c.1672A>C	ENSP00000295897.4:p.Lys558Gln
ENST00000401494.7:c.1327A>C	ENSP00000384695.3:p.Lys443Gln
ENST00000415165.6:c.1096A>C	ENSP00000401820.2:p.Lys366Gln
ENST00000476441.6:c.*951A>C	ENSP00000423727.1:n.*951A>C
ENST00000486939.1:n.326A>C
ENST00000503124.5:c.1222A>C	ENSP00000421027.1:p.Lys408Gln
ENST00000505649.5:n.1219A>C
ENST00000508932.5:n.175+71A>C
ENST00000509063.5:c.1672A>C	ENSP00000422784.1:p.Lys558Gln
ENST00000511370.1:c.1205A>C
ENST00000621085.4:c.1033A>C	ENSP00000483421.1:p.Lys345Gln
ENST00000621628.4:c.1033A>C	ENSP00000480485.1:p.Lys345Gln
NM_000477.5:c.1672A>C	NP_000468.1:p.Lys558Gln
NM_000477.6:c.1672A>C	NP_000468.1:p.Lys558Gln
NM_000477.7:c.1672A>C MANE Select	NP_000468.1:p.Lys558Gln