Canonical Allele Identifier: CA2655449396
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888358_20888361dup , CM000684.2:g.20888358_20888361dup GRCh38
NC_000022.10:g.21242646_21242649dup , CM000684.1:g.21242646_21242649dup GRCh37
NC_000022.9:g.19572646_19572649dup NCBI36
NG_012152.1:g.34355_34358dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*522_*525dup MANE Select ENSP00000215730.6:n.*522_*525dup
ENST00000215730.11:c.*522_*525dup ENSP00000215730.6:n.*522_*525dup
NM_004782.3:c.*522_*525dup NP_004773.1:n.*522_*525dup
NM_004782.4:c.*522_*525dup MANE Select NP_004773.1:n.*522_*525dup