Canonical Allele Identifier: CA2685803688
Gene: SHH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812251dup , CM000669.2:g.155812251dup GRCh38
NC_000007.13:g.155604945dup , CM000669.1:g.155604945dup GRCh37
NC_000007.12:g.155297706dup NCBI36
NG_007504.2:g.5023dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-129dup MANE Select ENSP00000297261.2:n.-129dup
ENST00000297261.6:c.-129dup ENSP00000297261.2:n.-129dup
NM_000193.2:c.-129dup NP_000184.1:n.-129dup
NM_000193.3:c.-129dup NP_000184.1:n.-129dup
NM_000193.4:c.-129dup MANE Select NP_000184.1:n.-129dup