Canonical Allele Identifier: CA2607855745

Gene: ALB

Linked Data

• dbSNP Id: rs2149327526
• gnomAD v4: 4-73408943-AAGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408948_73408950del , CM000666.2:g.73408948_73408950del	GRCh38
NC_000004.11:g.74274665_74274667del , CM000666.1:g.74274665_74274667del	GRCh37
NC_000004.10:g.74493529_74493531del	NCBI36
NG_009291.1:g.9694_9696del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+143_482+145del MANE Select	ENSP00000295897.4:n.482+143_482+145del
ENST00000295897.8:c.482+143_482+145del	ENSP00000295897.4:n.482+143_482+145del
ENST00000401494.7:c.138-407_138-405del	ENSP00000384695.3:n.138-407_138-405del
ENST00000415165.6:c.138-3048_138-3046del	ENSP00000401820.2:n.138-3048_138-3046del
ENST00000441319.5:c.488+143_488+145del	ENSP00000392541.1:n.488+143_488+145del
ENST00000476441.6:c.80-407_80-405del	ENSP00000423727.1:n.80-407_80-405del
ENST00000503124.5:c.33-407_33-405del	ENSP00000421027.1:n.33-407_33-405del
ENST00000505649.5:n.168+143_168+145del
ENST00000509063.5:c.482+143_482+145del	ENSP00000422784.1:n.482+143_482+145del
ENST00000514786.1:n.451+143_451+145del
ENST00000621085.4:c.482+143_482+145del	ENSP00000483421.1:n.482+143_482+145del
ENST00000621628.4:c.483-125_483-123del	ENSP00000480485.1:n.483-125_483-123del
NM_000477.5:c.482+143_482+145del	NP_000468.1:n.482+143_482+145del
NM_000477.6:c.482+143_482+145del	NP_000468.1:n.482+143_482+145del
NM_000477.7:c.482+143_482+145del MANE Select	NP_000468.1:n.482+143_482+145del