Canonical Allele Identifier: CA751562904

Gene: SNAP29

Linked Data

• dbSNP Id: rs1555915259
• MyVariant Identifiers: chr22:g.21242599_21242600insACACACACACAC (hg19) ; chr22:g.20888311_20888312insACACACACACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888311_20888312insACACACACACAC , CM000684.2:g.20888311_20888312insACACACACACAC	GRCh38
NC_000022.10:g.21242599_21242600insACACACACACAC , CM000684.1:g.21242599_21242600insACACACACACAC	GRCh37
NC_000022.9:g.19572599_19572600insACACACACACAC	NCBI36
NG_012152.1:g.34308_34309insACACACACACAC

Transcript Alleles

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