Canonical Allele Identifier: CA2578111805

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420304C>G , CM000666.2:g.73420304C>G	GRCh38
NC_000004.11:g.74286021C>G , CM000666.1:g.74286021C>G	GRCh37
NC_000004.10:g.74504885C>G	NCBI36
NG_009291.1:g.21050C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*6C>G MANE Select	ENSP00000295897.4:n.*6C>G
ENST00000295897.8:c.*6C>G	ENSP00000295897.4:n.*6C>G
ENST00000401494.7:c.*6C>G	ENSP00000384695.3:n.*6C>G
ENST00000415165.6:c.*6C>G	ENSP00000401820.2:n.*6C>G
ENST00000476441.6:c.*1115C>G	ENSP00000423727.1:n.*1115C>G
ENST00000495173.1:n.144C>G
ENST00000503124.5:c.*6C>G	ENSP00000421027.1:n.*6C>G
ENST00000505649.5:n.1383C>G
ENST00000508932.5:n.226C>G
ENST00000509063.5:c.1785+665C>G	ENSP00000422784.1:n.1785+665C>G
ENST00000511370.1:c.1369C>G
ENST00000621085.4:c.*6C>G	ENSP00000483421.1:n.*6C>G
ENST00000621628.4:c.*6C>G	ENSP00000480485.1:n.*6C>G
NM_000477.5:c.*6C>G	NP_000468.1:n.*6C>G
NM_000477.6:c.*6C>G	NP_000468.1:n.*6C>G
NM_000477.7:c.*6C>G MANE Select	NP_000468.1:n.*6C>G