Canonical Allele Identifier: CA1866666585
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851622_97851627delinsAGTTTT , CM000671.2:g.97851622_97851627delinsAGTTTT GRCh38
NC_000009.11:g.100613904_100613909delinsAGTTTT , CM000671.1:g.100613904_100613909delinsAGTTTT GRCh37
NC_000009.10:g.99653725_99653730delinsAGTTTT NCBI36
NG_011979.1:g.3368_3373delinsAGTTTT

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1249_218+1254delinsAAAACT
XR_930159.1:n.218+1249_218+1254delinsAAAACT
XR_930160.1:n.218+1249_218+1254delinsAAAACT
XR_930161.1:n.218+1249_218+1254delinsAAAACT
NR_147055.1:n.165+1289_165+1294delinsAAAACT