Canonical Allele Identifier: CA648963721

Gene: ALB

Linked Data

• COSMIC: COSN1300883

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419660_73419661dup , CM000666.2:g.73419660_73419661dup	GRCh38
NC_000004.11:g.74285377_74285378dup , CM000666.1:g.74285377_74285378dup	GRCh37
NC_000004.10:g.74504241_74504242dup	NCBI36
NG_009291.1:g.20406_20407dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1785+21_1785+22dup MANE Select	ENSP00000295897.4:n.1785+21_1785+22dup
ENST00000295897.8:c.1785+21_1785+22dup	ENSP00000295897.4:n.1785+21_1785+22dup
ENST00000401494.7:c.1440+21_1440+22dup	ENSP00000384695.3:n.1440+21_1440+22dup
ENST00000415165.6:c.1209+21_1209+22dup	ENSP00000401820.2:n.1209+21_1209+22dup
ENST00000476441.6:c.*1064+21_*1064+22dup	ENSP00000423727.1:n.*1064+21_*1064+22dup
ENST00000495173.1:n.93+21_93+22dup
ENST00000503124.5:c.1335+21_1335+22dup	ENSP00000421027.1:n.1335+21_1335+22dup
ENST00000505649.5:n.1332+21_1332+22dup
ENST00000508932.5:n.175+205_175+206dup
ENST00000509063.5:c.1785+21_1785+22dup	ENSP00000422784.1:n.1785+21_1785+22dup
ENST00000511370.1:c.1318+21_1318+22dup
ENST00000621085.4:c.1146+21_1146+22dup	ENSP00000483421.1:n.1146+21_1146+22dup
ENST00000621628.4:c.1146+21_1146+22dup	ENSP00000480485.1:n.1146+21_1146+22dup
NM_000477.5:c.1785+21_1785+22dup	NP_000468.1:n.1785+21_1785+22dup
NM_000477.6:c.1785+21_1785+22dup	NP_000468.1:n.1785+21_1785+22dup
NM_000477.7:c.1785+21_1785+22dup MANE Select	NP_000468.1:n.1785+21_1785+22dup