Canonical Allele Identifier: CA2655449344
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888311_20888312dup , CM000684.2:g.20888311_20888312dup GRCh38
NC_000022.10:g.21242599_21242600dup , CM000684.1:g.21242599_21242600dup GRCh37
NC_000022.9:g.19572599_19572600dup NCBI36
NG_012152.1:g.34308_34309dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*475_*476dup MANE Select ENSP00000215730.6:n.*475_*476dup
ENST00000215730.11:c.*475_*476dup ENSP00000215730.6:n.*475_*476dup
NM_004782.3:c.*475_*476dup NP_004773.1:n.*475_*476dup
NM_004782.4:c.*475_*476dup MANE Select NP_004773.1:n.*475_*476dup