Canonical Allele Identifier: CA2670937225

Gene: ALB

Linked Data

• gnomAD v4: 4-73409177-CCCTTTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409180_73409187del , CM000666.2:g.73409180_73409187del	GRCh38
NC_000004.11:g.74274897_74274904del , CM000666.1:g.74274897_74274904del	GRCh37
NC_000004.10:g.74493761_74493768del	NCBI36
NG_009291.1:g.9926_9933del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-175_483-168del MANE Select	ENSP00000295897.4:n.483-175_483-168del
ENST00000295897.8:c.483-175_483-168del	ENSP00000295897.4:n.483-175_483-168del
ENST00000401494.7:c.138-175_138-168del	ENSP00000384695.3:n.138-175_138-168del
ENST00000415165.6:c.138-2816_138-2809del	ENSP00000401820.2:n.138-2816_138-2809del
ENST00000441319.5:c.489-175_489-168del	ENSP00000392541.1:n.489-175_489-168del
ENST00000476441.6:c.80-175_80-168del	ENSP00000423727.1:n.80-175_80-168del
ENST00000503124.5:c.33-175_33-168del	ENSP00000421027.1:n.33-175_33-168del
ENST00000505649.5:n.169-175_169-168del
ENST00000509063.5:c.483-175_483-168del	ENSP00000422784.1:n.483-175_483-168del
ENST00000514786.1:n.452-175_452-168del
ENST00000621085.4:c.483-175_483-168del	ENSP00000483421.1:n.483-175_483-168del
ENST00000621628.4:c.486+104_486+111del	ENSP00000480485.1:n.486+104_486+111del
NM_000477.5:c.483-175_483-168del	NP_000468.1:n.483-175_483-168del
NM_000477.6:c.483-175_483-168del	NP_000468.1:n.483-175_483-168del
NM_000477.7:c.483-175_483-168del MANE Select	NP_000468.1:n.483-175_483-168del