Canonical Allele Identifier: CA2655449353
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888322_20888324del , CM000684.2:g.20888322_20888324del GRCh38
NC_000022.10:g.21242610_21242612del , CM000684.1:g.21242610_21242612del GRCh37
NC_000022.9:g.19572610_19572612del NCBI36
NG_012152.1:g.34319_34321del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*486_*488del MANE Select ENSP00000215730.6:n.*486_*488del
ENST00000215730.11:c.*486_*488del ENSP00000215730.6:n.*486_*488del
NM_004782.3:c.*486_*488del NP_004773.1:n.*486_*488del
NM_004782.4:c.*486_*488del MANE Select NP_004773.1:n.*486_*488del