Canonical Allele Identifier: CA1468152577

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409178_73409181delinsCCTT , CM000666.2:g.73409178_73409181delinsCCTT	GRCh38
NC_000004.11:g.74274895_74274898delinsCCTT , CM000666.1:g.74274895_74274898delinsCCTT	GRCh37
NC_000004.10:g.74493759_74493762delinsCCTT	NCBI36
NG_009291.1:g.9924_9927delinsCCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-177_483-174delinsCCTT MANE Select	ENSP00000295897.4:n.483-177_483-174delinsCCTT
ENST00000295897.8:c.483-177_483-174delinsCCTT	ENSP00000295897.4:n.483-177_483-174delinsCCTT
ENST00000401494.7:c.138-177_138-174delinsCCTT	ENSP00000384695.3:n.138-177_138-174delinsCCTT
ENST00000415165.6:c.138-2818_138-2815delinsCCTT	ENSP00000401820.2:n.138-2818_138-2815delinsCCTT
ENST00000441319.5:c.489-177_489-174delinsCCTT	ENSP00000392541.1:n.489-177_489-174delinsCCTT
ENST00000476441.6:c.80-177_80-174delinsCCTT	ENSP00000423727.1:n.80-177_80-174delinsCCTT
ENST00000503124.5:c.33-177_33-174delinsCCTT	ENSP00000421027.1:n.33-177_33-174delinsCCTT
ENST00000505649.5:n.169-177_169-174delinsCCTT
ENST00000509063.5:c.483-177_483-174delinsCCTT	ENSP00000422784.1:n.483-177_483-174delinsCCTT
ENST00000514786.1:n.452-177_452-174delinsCCTT
ENST00000621085.4:c.483-177_483-174delinsCCTT	ENSP00000483421.1:n.483-177_483-174delinsCCTT
ENST00000621628.4:c.486+102_486+105delinsCCTT	ENSP00000480485.1:n.486+102_486+105delinsCCTT
NM_000477.5:c.483-177_483-174delinsCCTT	NP_000468.1:n.483-177_483-174delinsCCTT
NM_000477.6:c.483-177_483-174delinsCCTT	NP_000468.1:n.483-177_483-174delinsCCTT
NM_000477.7:c.483-177_483-174delinsCCTT MANE Select	NP_000468.1:n.483-177_483-174delinsCCTT