Canonical Allele Identifier: CA1282423169

Gene: CCDC93

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118005492G>C , CM000664.2:g.118005492G>C	GRCh38
NC_000002.11:g.118763068G>C , CM000664.1:g.118763068G>C	GRCh37
NC_000002.10:g.118479538G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376300.7:c.251+1230C>G MANE Select	ENSP00000365477.2:n.251+1230C>G
ENST00000319432.9:c.251+1230C>G	ENSP00000324135.5:n.251+1230C>G
ENST00000376300.6:c.251+1230C>G	ENSP00000365477.2:n.251+1230C>G
NM_019044.4:c.251+1230C>G	NP_061917.3:n.251+1230C>G
XM_006712600.2:c.419+1230C>G	XP_006712663.1:n.419+1230C>G
XM_011511359.1:c.419+1230C>G	XP_011509661.1:n.419+1230C>G
XM_011511360.1:c.419+1230C>G	XP_011509662.1:n.419+1230C>G
XM_011511361.1:c.-121-708C>G	XP_011509663.1:n.-121-708C>G
XM_011511362.1:c.-37+1230C>G	XP_011509664.1:n.-37+1230C>G
XM_011511363.1:c.419+1230C>G	XP_011509665.1:n.419+1230C>G
XM_011511363.2:c.419+1230C>G	XP_011509665.1:n.419+1230C>G
NM_019044.5:c.251+1230C>G MANE Select	NP_061917.3:n.251+1230C>G