Canonical Allele Identifier: CA2396589608

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888341_20888357delinsACACACACACACACACT , CM000684.2:g.20888341_20888357delinsACACACACACACACACT	GRCh38
NC_000022.10:g.21242629_21242645delinsACACACACACACACACT , CM000684.1:g.21242629_21242645delinsACACACACACACACACT	GRCh37
NC_000022.9:g.19572629_19572645delinsACACACACACACACACT	NCBI36
NG_012152.1:g.34338_34354delinsACACACACACACACACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*505_*521delinsACACACACACACACACT MANE Select	ENSP00000215730.6:n.*505_*521delinsACACACACACACACACT
ENST00000215730.11:c.*505_*521delinsACACACACACACACACT	ENSP00000215730.6:n.*505_*521delinsACACACACACACACACT
NM_004782.3:c.*505_*521delinsACACACACACACACACT	NP_004773.1:n.*505_*521delinsACACACACACACACACT
NM_004782.4:c.*505_*521delinsACACACACACACACACT MANE Select	NP_004773.1:n.*505_*521delinsACACACACACACACACT