Canonical Allele Identifier: CA2762164328

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408975_73408976del , CM000666.2:g.73408975_73408976del	GRCh38
NC_000004.11:g.74274692_74274693del , CM000666.1:g.74274692_74274693del	GRCh37
NC_000004.10:g.74493556_74493557del	NCBI36
NG_009291.1:g.9721_9722del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+170_482+171del MANE Select	ENSP00000295897.4:n.482+170_482+171del
ENST00000295897.8:c.482+170_482+171del	ENSP00000295897.4:n.482+170_482+171del
ENST00000401494.7:c.138-380_138-379del	ENSP00000384695.3:n.138-380_138-379del
ENST00000415165.6:c.138-3021_138-3020del	ENSP00000401820.2:n.138-3021_138-3020del
ENST00000441319.5:c.488+170_488+171del	ENSP00000392541.1:n.488+170_488+171del
ENST00000476441.6:c.80-380_80-379del	ENSP00000423727.1:n.80-380_80-379del
ENST00000503124.5:c.33-380_33-379del	ENSP00000421027.1:n.33-380_33-379del
ENST00000505649.5:n.168+170_168+171del
ENST00000509063.5:c.482+170_482+171del	ENSP00000422784.1:n.482+170_482+171del
ENST00000514786.1:n.451+170_451+171del
ENST00000621085.4:c.482+170_482+171del	ENSP00000483421.1:n.482+170_482+171del
ENST00000621628.4:c.483-98_483-97del	ENSP00000480485.1:n.483-98_483-97del
NM_000477.5:c.482+170_482+171del	NP_000468.1:n.482+170_482+171del
NM_000477.6:c.482+170_482+171del	NP_000468.1:n.482+170_482+171del
NM_000477.7:c.482+170_482+171del MANE Select	NP_000468.1:n.482+170_482+171del