Canonical Allele Identifier: CA2396589569
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929069148

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888311_20888316del , CM000684.2:g.20888311_20888316del GRCh38
NC_000022.10:g.21242599_21242604del , CM000684.1:g.21242599_21242604del GRCh37
NC_000022.9:g.19572599_19572604del NCBI36
NG_012152.1:g.34308_34313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*475_*480del MANE Select ENSP00000215730.6:n.*475_*480del
ENST00000215730.11:c.*475_*480del ENSP00000215730.6:n.*475_*480del
NM_004782.3:c.*475_*480del NP_004773.1:n.*475_*480del
NM_004782.4:c.*475_*480del MANE Select NP_004773.1:n.*475_*480del