Canonical Allele Identifier: CA2655449384
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888343_20888349del , CM000684.2:g.20888343_20888349del GRCh38
NC_000022.10:g.21242631_21242637del , CM000684.1:g.21242631_21242637del GRCh37
NC_000022.9:g.19572631_19572637del NCBI36
NG_012152.1:g.34340_34346del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*507_*513del MANE Select ENSP00000215730.6:n.*507_*513del
ENST00000215730.11:c.*507_*513del ENSP00000215730.6:n.*507_*513del
NM_004782.3:c.*507_*513del NP_004773.1:n.*507_*513del
NM_004782.4:c.*507_*513del MANE Select NP_004773.1:n.*507_*513del