Canonical Allele Identifier: CA2260368520
Gene: HCRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184708_42184711delinsCCTT , CM000679.2:g.42184708_42184711delinsCCTT GRCh38
NC_000017.10:g.40336726_40336729delinsCCTT , CM000679.1:g.40336726_40336729delinsCCTT GRCh37
NC_000017.9:g.37590252_37590255delinsCCTT NCBI36
NG_011448.1:g.5742_5745delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-183_22-180delinsAAGG MANE Select ENSP00000293330.1:n.22-183_22-180delinsAAGG
NM_001524.1:c.22-183_22-180delinsAAGG MANE Select NP_001515.1:n.22-183_22-180delinsAAGG