Canonical Allele Identifier: CA2778560918
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812332_155812333insAAACA , CM000669.2:g.155812332_155812333insAAACA GRCh38
NC_000007.13:g.155605026_155605027insAAACA , CM000669.1:g.155605026_155605027insAAACA GRCh37
NC_000007.12:g.155297787_155297788insAAACA NCBI36
NG_007504.2:g.4941_4942insTGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-211_-210insTGTTT MANE Select ENSP00000297261.2:n.-211_-210insTGTTT
NM_000193.4:c.-211_-210insTGTTT MANE Select NP_000184.1:n.-211_-210insTGTTT