Canonical Allele Identifier: CA2567673158
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851935_97851936insGGGGGGGGGGGG , CM000671.2:g.97851935_97851936insGGGGGGGGGGGG GRCh38
NC_000009.11:g.100614217_100614218insGGGGGGGGGGGG , CM000671.1:g.100614217_100614218insGGGGGGGGGGGG GRCh37
NC_000009.10:g.99654038_99654039insGGGGGGGGGGGG NCBI36
NG_011979.1:g.3681_3682insGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+942_218+943insCCCCCCCCCCCC
XR_930159.1:n.218+942_218+943insCCCCCCCCCCCC
XR_930160.1:n.218+942_218+943insCCCCCCCCCCCC
XR_930161.1:n.218+942_218+943insCCCCCCCCCCCC
NR_147055.1:n.165+982_165+983insCCCCCCCCCCCC