Canonical Allele Identifier: CA2670965587

Gene: ALB

Linked Data

• gnomAD v4: 4-73415234-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415235_73415236dup , CM000666.2:g.73415235_73415236dup	GRCh38
NC_000004.11:g.74280952_74280953dup , CM000666.1:g.74280952_74280953dup	GRCh37
NC_000004.10:g.74499816_74499817dup	NCBI36
NG_009291.1:g.15981_15982dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+68_1191+69dup MANE Select	ENSP00000295897.4:n.1191+68_1191+69dup
ENST00000295897.8:c.1191+68_1191+69dup	ENSP00000295897.4:n.1191+68_1191+69dup
ENST00000401494.7:c.846+68_846+69dup	ENSP00000384695.3:n.846+68_846+69dup
ENST00000415165.6:c.615+68_615+69dup	ENSP00000401820.2:n.615+68_615+69dup
ENST00000476441.6:c.*470+68_*470+69dup	ENSP00000423727.1:n.*470+68_*470+69dup
ENST00000484992.1:n.511+68_511+69dup
ENST00000503124.5:c.741+68_741+69dup	ENSP00000421027.1:n.741+68_741+69dup
ENST00000504043.1:n.262_263dup
ENST00000505649.5:n.877+68_877+69dup
ENST00000509063.5:c.1191+68_1191+69dup	ENSP00000422784.1:n.1191+68_1191+69dup
ENST00000511370.1:c.724+68_724+69dup
ENST00000621085.4:c.552+68_552+69dup	ENSP00000483421.1:n.552+68_552+69dup
ENST00000621628.4:c.552+68_552+69dup	ENSP00000480485.1:n.552+68_552+69dup
NM_000477.5:c.1191+68_1191+69dup	NP_000468.1:n.1191+68_1191+69dup
NM_000477.6:c.1191+68_1191+69dup	NP_000468.1:n.1191+68_1191+69dup
NM_000477.7:c.1191+68_1191+69dup MANE Select	NP_000468.1:n.1191+68_1191+69dup