Canonical Allele Identifier: CA2818431278

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888476_20888477insTGT , CM000684.2:g.20888476_20888477insTGT	GRCh38
NC_000022.10:g.21242764_21242765insTGT , CM000684.1:g.21242764_21242765insTGT	GRCh37
NC_000022.9:g.19572764_19572765insTGT	NCBI36
NG_012152.1:g.34473_34474insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*640_*641insTGT MANE Select	ENSP00000215730.6:n.*640_*641insTGT
ENST00000215730.11:c.*640_*641insTGT	ENSP00000215730.6:n.*640_*641insTGT
NM_004782.3:c.*640_*641insTGT	NP_004773.1:n.*640_*641insTGT
NM_004782.4:c.*640_*641insTGT MANE Select	NP_004773.1:n.*640_*641insTGT