Canonical Allele Identifier: CA1024230600
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888321_20888356dup , CM000684.2:g.20888321_20888356dup GRCh38
NC_000022.10:g.21242609_21242644dup , CM000684.1:g.21242609_21242644dup GRCh37
NC_000022.9:g.19572609_19572644dup NCBI36
NG_012152.1:g.34318_34353dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*485_*520dup MANE Select ENSP00000215730.6:n.*485_*520dup
ENST00000215730.11:c.*485_*520dup ENSP00000215730.6:n.*485_*520dup
NM_004782.3:c.*485_*520dup NP_004773.1:n.*485_*520dup
NM_004782.4:c.*485_*520dup MANE Select NP_004773.1:n.*485_*520dup