Canonical Allele Identifier: CA1246500878
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731821_39731825delinsTTCTG , CM000664.2:g.39731821_39731825delinsTTCTG GRCh38
NC_000002.11:g.39958961_39958965delinsTTCTG , CM000664.1:g.39958961_39958965delinsTTCTG GRCh37
NC_000002.10:g.39812465_39812469delinsTTCTG NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3408_401-3404delinsTTCTG XP_024308470.1:n.401-3408_401-3404delinsT...