Canonical Allele Identifier: CA2396589402

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20887960_20887961delinsAG , CM000684.2:g.20887960_20887961delinsAG	GRCh38
NC_000022.10:g.21242248_21242249delinsAG , CM000684.1:g.21242248_21242249delinsAG	GRCh37
NC_000022.9:g.19572248_19572249delinsAG	NCBI36
NG_012152.1:g.33957_33958delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*124_*125delinsAG MANE Select	ENSP00000215730.6:n.*124_*125delinsAG
ENST00000215730.11:c.*124_*125delinsAG	ENSP00000215730.6:n.*124_*125delinsAG
NM_004782.3:c.*124_*125delinsAG	NP_004773.1:n.*124_*125delinsAG
NM_004782.4:c.*124_*125delinsAG MANE Select	NP_004773.1:n.*124_*125delinsAG