Canonical Allele Identifier: CA652293179
Gene: SHH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812216dup , CM000669.2:g.155812216dup GRCh38
NC_000007.13:g.155604910dup , CM000669.1:g.155604910dup GRCh37
NC_000007.12:g.155297671dup NCBI36
NG_007504.2:g.5058dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-94dup MANE Select ENSP00000297261.2:n.-94dup
ENST00000297261.6:c.-94dup ENSP00000297261.2:n.-94dup
NM_000193.2:c.-94dup NP_000184.1:n.-94dup
NM_000193.3:c.-94dup NP_000184.1:n.-94dup
NM_000193.4:c.-94dup MANE Select NP_000184.1:n.-94dup