Canonical Allele Identifier: CA2396589626
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888351_20888359delinsACACACTCT , CM000684.2:g.20888351_20888359delinsACACACTCT GRCh38
NC_000022.10:g.21242639_21242647delinsACACACTCT , CM000684.1:g.21242639_21242647delinsACACACTCT GRCh37
NC_000022.9:g.19572639_19572647delinsACACACTCT NCBI36
NG_012152.1:g.34348_34356delinsACACACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*515_*523delinsACACACTCT MANE Select ENSP00000215730.6:n.*515_*523delinsACACACTCT
ENST00000215730.11:c.*515_*523delinsACACACTCT ENSP00000215730.6:n.*515_*523delinsACACACTCT
NM_004782.3:c.*515_*523delinsACACACTCT NP_004773.1:n.*515_*523delinsACACACTCT
NM_004782.4:c.*515_*523delinsACACACTCT MANE Select NP_004773.1:n.*515_*523delinsACACACTCT