Canonical Allele Identifier: CA2396589468
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888093A= , CM000684.2:g.20888093A= GRCh38
NC_000022.10:g.21242381A= , CM000684.1:g.21242381A= GRCh37
NC_000022.9:g.19572381A= NCBI36
NG_012152.1:g.34090A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*257A= MANE Select ENSP00000215730.6:n.*257A=
ENST00000215730.11:c.*257A= ENSP00000215730.6:n.*257A=
NM_004782.3:c.*257A= NP_004773.1:n.*257A=
NM_004782.4:c.*257A= MANE Select NP_004773.1:n.*257A=
Search 100 bp 5'
Search 100 bp 3'