Canonical Allele Identifier: CA2670966779

Gene: ALB

Linked Data

• gnomAD v4: 4-73420319-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420319C>A , CM000666.2:g.73420319C>A	GRCh38
NC_000004.11:g.74286036C>A , CM000666.1:g.74286036C>A	GRCh37
NC_000004.10:g.74504900C>A	NCBI36
NG_009291.1:g.21065C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*21C>A MANE Select	ENSP00000295897.4:n.*21C>A
ENST00000295897.8:c.*21C>A	ENSP00000295897.4:n.*21C>A
ENST00000401494.7:c.*21C>A	ENSP00000384695.3:n.*21C>A
ENST00000415165.6:c.*21C>A	ENSP00000401820.2:n.*21C>A
ENST00000476441.6:c.*1130C>A	ENSP00000423727.1:n.*1130C>A
ENST00000495173.1:n.159C>A
ENST00000503124.5:c.*21C>A	ENSP00000421027.1:n.*21C>A
ENST00000505649.5:n.1398C>A
ENST00000508932.5:n.241C>A
ENST00000509063.5:c.1785+680C>A	ENSP00000422784.1:n.1785+680C>A
ENST00000511370.1:c.1384C>A
ENST00000621085.4:c.*21C>A	ENSP00000483421.1:n.*21C>A
ENST00000621628.4:c.*21C>A	ENSP00000480485.1:n.*21C>A
NM_000477.5:c.*21C>A	NP_000468.1:n.*21C>A
NM_000477.6:c.*21C>A	NP_000468.1:n.*21C>A
NM_000477.7:c.*21C>A MANE Select	NP_000468.1:n.*21C>A