Canonical Allele Identifier: CA99712633

Gene: ALB

Linked Data

• dbSNP Id: rs867670544
• MyVariant Identifiers: chr4:g.74285987C>A (hg19) ; chr4:g.73420270C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420270C>A , CM000666.2:g.73420270C>A	GRCh38
NC_000004.11:g.74285987C>A , CM000666.1:g.74285987C>A	GRCh37
NC_000004.10:g.74504851C>A	NCBI36
NG_009291.1:g.21016C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1802C>A MANE Select	ENSP00000295897.4:p.Ala601Asp
ENST00000295897.8:c.1802C>A	ENSP00000295897.4:p.Ala601Asp
ENST00000401494.7:c.1457C>A	ENSP00000384695.3:p.Ala486Asp
ENST00000415165.6:c.1226C>A	ENSP00000401820.2:p.Ala409Asp
ENST00000476441.6:c.*1081C>A	ENSP00000423727.1:n.*1081C>A
ENST00000495173.1:n.110C>A
ENST00000503124.5:c.1352C>A	ENSP00000421027.1:p.Ala451Asp
ENST00000505649.5:n.1349C>A
ENST00000508932.5:n.192C>A
ENST00000509063.5:c.1785+631C>A	ENSP00000422784.1:n.1785+631C>A
ENST00000511370.1:c.1335C>A
ENST00000621085.4:c.1163C>A	ENSP00000483421.1:p.Ala388Asp
ENST00000621628.4:c.1163C>A	ENSP00000480485.1:p.Ala388Asp
NM_000477.5:c.1802C>A	NP_000468.1:p.Ala601Asp
NM_000477.6:c.1802C>A	NP_000468.1:p.Ala601Asp
NM_000477.7:c.1802C>A MANE Select	NP_000468.1:p.Ala601Asp