Canonical Allele Identifier: CA2578111804

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420299C>T , CM000666.2:g.73420299C>T	GRCh38
NC_000004.11:g.74286016C>T , CM000666.1:g.74286016C>T	GRCh37
NC_000004.10:g.74504880C>T	NCBI36
NG_009291.1:g.21045C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*1C>T MANE Select	ENSP00000295897.4:n.*1C>T
ENST00000295897.8:c.*1C>T	ENSP00000295897.4:n.*1C>T
ENST00000401494.7:c.*1C>T	ENSP00000384695.3:n.*1C>T
ENST00000415165.6:c.*1C>T	ENSP00000401820.2:n.*1C>T
ENST00000476441.6:c.*1110C>T	ENSP00000423727.1:n.*1110C>T
ENST00000495173.1:n.139C>T
ENST00000503124.5:c.*1C>T	ENSP00000421027.1:n.*1C>T
ENST00000505649.5:n.1378C>T
ENST00000508932.5:n.221C>T
ENST00000509063.5:c.1785+660C>T	ENSP00000422784.1:n.1785+660C>T
ENST00000511370.1:c.1364C>T
ENST00000621085.4:c.*1C>T	ENSP00000483421.1:n.*1C>T
ENST00000621628.4:c.*1C>T	ENSP00000480485.1:n.*1C>T
NM_000477.5:c.*1C>T	NP_000468.1:n.*1C>T
NM_000477.6:c.*1C>T	NP_000468.1:n.*1C>T
NM_000477.7:c.*1C>T MANE Select	NP_000468.1:n.*1C>T