Canonical Allele Identifier: CA10673104
Gene: C1orf168 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17372114

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56777781T>C , CM000663.2:g.56777781T>C GRCh38
NC_000001.10:g.57243454T>C , CM000663.1:g.57243454T>C GRCh37
NC_000001.9:g.57016042T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001004303.4:c.953+9394A>G VV NP_001004303.3:p.=
XM_005270584.3:c.953+9394A>G XP_005270641.1:p.=
XM_011540898.1:c.953+9394A>G XP_011539200.1:p.=
XM_011540899.1:c.953+9394A>G XP_011539201.1:p.=
XM_011540900.1:c.953+9394A>G XP_011539202.1:p.=
XM_011540901.1:c.953+9394A>G XP_011539203.1:p.=
XM_011540902.1:c.953+9394A>G XP_011539204.1:p.=
XM_011540903.1:c.953+9394A>G XP_011539205.1:p.=
XM_011540905.1:c.953+9394A>G XP_011539207.1:p.=
XM_011540907.1:c.953+9394A>G XP_011539209.1:p.=
XR_946569.1:n.1359+9394A>G
XR_946570.1:n.1359+9394A>G
XR_946571.1:n.1359+9394A>G
XR_946572.1:n.1359+9394A>G
XM_011540900.2:c.953+9394A>G XP_011539202.1:p.=
XM_011540903.2:c.953+9394A>G XP_011539205.1:p.=
XM_011540905.2:c.953+9394A>G XP_011539207.1:p.=
XM_017000544.2:c.563+9394A>G XP_016856033.1:p.=
XM_017000545.1:c.563+9394A>G XP_016856034.1:p.=
XM_017000548.1:c.953+9394A>G XP_016856037.1:p.=
XM_024453853.1:c.953+9394A>G XP_024309621.1:p.=
XR_001737026.1:n.1359+9394A>G
XR_946572.2:n.1359+9394A>G
NM_001004303.5:c.953+9394A>G VV MANE Preferred NP_001004303.3:p.=
ENST00000343433.6:c.953+9394A>G ENSP00000345972.6:p.=
ENST00000484327.1:n.1359+9394A>G