Canonical Allele Identifier: CA2818431189
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888309_20888311del , CM000684.2:g.20888309_20888311del GRCh38
NC_000022.10:g.21242597_21242599del , CM000684.1:g.21242597_21242599del GRCh37
NC_000022.9:g.19572597_19572599del NCBI36
NG_012152.1:g.34306_34308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*473_*475del MANE Select ENSP00000215730.6:n.*473_*475del
ENST00000215730.11:c.*473_*475del ENSP00000215730.6:n.*473_*475del
NM_004782.3:c.*473_*475del NP_004773.1:n.*473_*475del
NM_004782.4:c.*473_*475del MANE Select NP_004773.1:n.*473_*475del