Canonical Allele Identifier: CA2581073202

Gene: C12orf60 SMCO3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14813670C>A , CM000674.2:g.14813670C>A	GRCh38
NC_000012.11:g.14966604C>A , CM000674.1:g.14966604C>A	GRCh37
NC_000012.10:g.14857871C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330828.3:c.-24-9242C>A (C12orf60) MANE Select	ENSP00000331691.2:n.-24-9242C>A
ENST00000648334.1:n.83+9919C>A (C12orf60)
ENST00000316048.2:c.-17+456G>T (SMCO3) MANE Select	ENSP00000381895.1:n.-17+456G>T
ENST00000330828.2:c.-24-9242C>A (C12orf60)	ENSP00000331691.2:n.-24-9242C>A
ENST00000527783.1:n.75+9919C>A (C12orf60)
ENST00000533472.1:n.86+9919C>A (C12orf60)
NM_001013698.2:c.-17+456G>T (SMCO3) MANE Select	NP_001013720.2:n.-17+456G>T
NM_175874.3:c.-24-9242C>A (C12orf60)	NP_787070.2:n.-24-9242C>A
XM_005253322.3:c.-24-9242C>A (C12orf60)	XP_005253379.1:n.-24-9242C>A
XM_005253323.2:c.-24-9242C>A (C12orf60)	XP_005253380.1:n.-24-9242C>A
XM_011520568.1:c.-25+2278C>A (C12orf60)	XP_011518870.1:n.-25+2278C>A
XM_011520569.1:c.-25+3242C>A (C12orf60)	XP_011518871.1:n.-25+3242C>A
XM_005253322.4:c.-24-9242C>A (C12orf60)	XP_005253379.1:n.-24-9242C>A
XM_011520568.2:c.-25+2278C>A (C12orf60)	XP_011518870.1:n.-25+2278C>A
XM_011520569.2:c.-25+3242C>A (C12orf60)	XP_011518871.1:n.-25+3242C>A
XM_017018873.1:c.-24-9242C>A (C12orf60)	XP_016874362.1:n.-24-9242C>A
XM_017018874.1:c.-24-9242C>A (C12orf60)	XP_016874363.1:n.-24-9242C>A
XM_017019312.1:c.-103+456G>T (SMCO3)	XP_016874801.1:n.-103+456G>T
XM_024448858.1:c.-24-9242C>A (C12orf60)	XP_024304626.1:n.-24-9242C>A
XM_024448859.1:c.-24-9242C>A (C12orf60)	XP_024304627.1:n.-24-9242C>A
NM_175874.4:c.-24-9242C>A (C12orf60) MANE Select	NP_787070.2:n.-24-9242C>A