Canonical Allele Identifier: CA1468152426

Gene: ALB

Linked Data

• dbSNP Id: rs1718799092
• gnomAD v4: 4-73408877-A-AATT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408879_73408881dup , CM000666.2:g.73408879_73408881dup	GRCh38
NC_000004.11:g.74274596_74274598dup , CM000666.1:g.74274596_74274598dup	GRCh37
NC_000004.10:g.74493460_74493462dup	NCBI36
NG_009291.1:g.9625_9627dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+74_482+76dup MANE Select	ENSP00000295897.4:n.482+74_482+76dup
ENST00000295897.8:c.482+74_482+76dup	ENSP00000295897.4:n.482+74_482+76dup
ENST00000401494.7:c.138-476_138-474dup	ENSP00000384695.3:n.138-476_138-474dup
ENST00000415165.6:c.138-3117_138-3115dup	ENSP00000401820.2:n.138-3117_138-3115dup
ENST00000441319.5:c.488+74_488+76dup	ENSP00000392541.1:n.488+74_488+76dup
ENST00000476441.6:c.80-476_80-474dup	ENSP00000423727.1:n.80-476_80-474dup
ENST00000503124.5:c.33-476_33-474dup	ENSP00000421027.1:n.33-476_33-474dup
ENST00000505649.5:n.168+74_168+76dup
ENST00000509063.5:c.482+74_482+76dup	ENSP00000422784.1:n.482+74_482+76dup
ENST00000514786.1:n.451+74_451+76dup
ENST00000515133.5:n.597_599dup
ENST00000621085.4:c.482+74_482+76dup	ENSP00000483421.1:n.482+74_482+76dup
ENST00000621628.4:c.482+74_482+76dup	ENSP00000480485.1:n.482+74_482+76dup
NM_000477.5:c.482+74_482+76dup	NP_000468.1:n.482+74_482+76dup
NM_000477.6:c.482+74_482+76dup	NP_000468.1:n.482+74_482+76dup
NM_000477.7:c.482+74_482+76dup MANE Select	NP_000468.1:n.482+74_482+76dup