Canonical Allele Identifier: CA357247070

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285977A>C (hg19) ; chr4:g.73420260A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420260A>C , CM000666.2:g.73420260A>C	GRCh38
NC_000004.11:g.74285977A>C , CM000666.1:g.74285977A>C	GRCh37
NC_000004.10:g.74504841A>C	NCBI36
NG_009291.1:g.21006A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1792A>C MANE Select	ENSP00000295897.4:p.Lys598Gln
ENST00000295897.8:c.1792A>C	ENSP00000295897.4:p.Lys598Gln
ENST00000401494.7:c.1447A>C	ENSP00000384695.3:p.Lys483Gln
ENST00000415165.6:c.1216A>C	ENSP00000401820.2:p.Lys406Gln
ENST00000476441.6:c.*1071A>C	ENSP00000423727.1:n.*1071A>C
ENST00000495173.1:n.100A>C
ENST00000503124.5:c.1342A>C	ENSP00000421027.1:p.Lys448Gln
ENST00000505649.5:n.1339A>C
ENST00000508932.5:n.182A>C
ENST00000509063.5:c.1785+621A>C	ENSP00000422784.1:n.1785+621A>C
ENST00000511370.1:c.1325A>C
ENST00000621085.4:c.1153A>C	ENSP00000483421.1:p.Lys385Gln
ENST00000621628.4:c.1153A>C	ENSP00000480485.1:p.Lys385Gln
NM_000477.5:c.1792A>C	NP_000468.1:p.Lys598Gln
NM_000477.6:c.1792A>C	NP_000468.1:p.Lys598Gln
NM_000477.7:c.1792A>C MANE Select	NP_000468.1:p.Lys598Gln