Canonical Allele Identifier: CA2655449489

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20888460-CGCTTCCCTCCAGCCCCCCATCCTTGGCATGTATATTAGTAGGAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888466_20888510del , CM000684.2:g.20888466_20888510del	GRCh38
NC_000022.10:g.21242754_21242798del , CM000684.1:g.21242754_21242798del	GRCh37
NC_000022.9:g.19572754_19572798del	NCBI36
NG_012152.1:g.34463_34507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*630_*674del MANE Select	ENSP00000215730.6:n.*630_*674del
ENST00000215730.11:c.*630_*674del	ENSP00000215730.6:n.*630_*674del
NM_004782.3:c.*630_*674del	NP_004773.1:n.*630_*674del
NM_004782.4:c.*630_*674del MANE Select	NP_004773.1:n.*630_*674del