Canonical Allele Identifier: CA1064142560

Gene: ALB

Linked Data

• dbSNP Id: rs1719099038
• gnomAD v3: 4-73419644-T-TAC
• gnomAD v4: 4-73419644-T-TAC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419646_73419647dup , CM000666.2:g.73419646_73419647dup	GRCh38
NC_000004.11:g.74285363_74285364dup , CM000666.1:g.74285363_74285364dup	GRCh37
NC_000004.10:g.74504227_74504228dup	NCBI36
NG_009291.1:g.20392_20393dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1785+7_1785+8dup MANE Select	ENSP00000295897.4:n.1785+7_1785+8dup
ENST00000295897.8:c.1785+7_1785+8dup	ENSP00000295897.4:n.1785+7_1785+8dup
ENST00000401494.7:c.1440+7_1440+8dup	ENSP00000384695.3:n.1440+7_1440+8dup
ENST00000415165.6:c.1209+7_1209+8dup	ENSP00000401820.2:n.1209+7_1209+8dup
ENST00000476441.6:c.*1064+7_*1064+8dup	ENSP00000423727.1:n.*1064+7_*1064+8dup
ENST00000495173.1:n.93+7_93+8dup
ENST00000503124.5:c.1335+7_1335+8dup	ENSP00000421027.1:n.1335+7_1335+8dup
ENST00000505649.5:n.1332+7_1332+8dup
ENST00000508932.5:n.175+191_175+192dup
ENST00000509063.5:c.1785+7_1785+8dup	ENSP00000422784.1:n.1785+7_1785+8dup
ENST00000511370.1:c.1318+7_1318+8dup
ENST00000621085.4:c.1146+7_1146+8dup	ENSP00000483421.1:n.1146+7_1146+8dup
ENST00000621628.4:c.1146+7_1146+8dup	ENSP00000480485.1:n.1146+7_1146+8dup
NM_000477.5:c.1785+7_1785+8dup	NP_000468.1:n.1785+7_1785+8dup
NM_000477.6:c.1785+7_1785+8dup	NP_000468.1:n.1785+7_1785+8dup
NM_000477.7:c.1785+7_1785+8dup MANE Select	NP_000468.1:n.1785+7_1785+8dup