Canonical Allele Identifier: CA2396589711

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888517_20888524delinsGCACTGCT , CM000684.2:g.20888517_20888524delinsGCACTGCT	GRCh38
NC_000022.10:g.21242805_21242812delinsGCACTGCT , CM000684.1:g.21242805_21242812delinsGCACTGCT	GRCh37
NC_000022.9:g.19572805_19572812delinsGCACTGCT	NCBI36
NG_012152.1:g.34514_34521delinsGCACTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*681_*688delinsGCACTGCT MANE Select	ENSP00000215730.6:n.*681_*688delinsGCACTGCT
ENST00000215730.11:c.*681_*688delinsGCACTGCT	ENSP00000215730.6:n.*681_*688delinsGCACTGCT
NM_004782.3:c.*681_*688delinsGCACTGCT	NP_004773.1:n.*681_*688delinsGCACTGCT
NM_004782.4:c.*681_*688delinsGCACTGCT MANE Select	NP_004773.1:n.*681_*688delinsGCACTGCT