Canonical Allele Identifier: CA2396589642

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888363_20888364delinsAG , CM000684.2:g.20888363_20888364delinsAG	GRCh38
NC_000022.10:g.21242651_21242652delinsAG , CM000684.1:g.21242651_21242652delinsAG	GRCh37
NC_000022.9:g.19572651_19572652delinsAG	NCBI36
NG_012152.1:g.34360_34361delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*527_*528delinsAG MANE Select	ENSP00000215730.6:n.*527_*528delinsAG
ENST00000215730.11:c.*527_*528delinsAG	ENSP00000215730.6:n.*527_*528delinsAG
NM_004782.3:c.*527_*528delinsAG	NP_004773.1:n.*527_*528delinsAG
NM_004782.4:c.*527_*528delinsAG MANE Select	NP_004773.1:n.*527_*528delinsAG