Canonical Allele Identifier: CA2396589446

Gene: SNAP29

Linked Data

• dbSNP Id: rs1929062177

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888054_20888055insTAAA , CM000684.2:g.20888054_20888055insTAAA	GRCh38
NC_000022.10:g.21242342_21242343insTAAA , CM000684.1:g.21242342_21242343insTAAA	GRCh37
NC_000022.9:g.19572342_19572343insTAAA	NCBI36
NG_012152.1:g.34051_34052insTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*218_*219insTAAA MANE Select	ENSP00000215730.6:n.*218_*219insTAAA
ENST00000215730.11:c.*218_*219insTAAA	ENSP00000215730.6:n.*218_*219insTAAA
NM_004782.3:c.*218_*219insTAAA	NP_004773.1:n.*218_*219insTAAA
NM_004782.4:c.*218_*219insTAAA MANE Select	NP_004773.1:n.*218_*219insTAAA