Canonical Allele Identifier: CA471183040

Gene: SEMA4G MRPL43 MIR608

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100975021C>T , CM000672.2:g.100975021C>T	GRCh38
NC_000010.10:g.102734778C>T , CM000672.1:g.102734778C>T	GRCh37
NC_000010.9:g.102724768C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210633.4:c.336+1412C>T (SEMA4G) MANE Select	ENSP00000210633.3:n.336+1412C>T
ENST00000476171.2:c.336+1412C>T (SEMA4G)	ENSP00000429888.2:n.336+1412C>T
ENST00000210633.3:c.336+1412C>T (SEMA4G)	ENSP00000210633.3:n.336+1412C>T
ENST00000370250.8:c.336+1412C>T (SEMA4G)	ENSP00000359270.4:n.336+1412C>T
ENST00000517724.5:c.336+1412C>T (SEMA4G)	ENSP00000430175.1:n.336+1412C>T
ENST00000518124.5:c.336+1412C>T (SEMA4G)	ENSP00000430103.1:n.336+1412C>T
ENST00000519649.5:c.336+1412C>T (SEMA4G)	ENSP00000428896.1:n.336+1412C>T
ENST00000519756.1:n.254+1412C>T (SEMA4G)
ENST00000521006.5:c.336+1412C>T (SEMA4G)	ENSP00000430881.1:n.336+1412C>T
ENST00000523148.5:c.398-5117G>A (MRPL43)
NM_001203244.1:c.336+1412C>T (SEMA4G)	NP_001190173.1:n.336+1412C>T
NM_017893.3:c.336+1412C>T (SEMA4G)	NP_060363.2:n.336+1412C>T
NR_030339.1:n.37C>T (MIR608)
XM_005270008.1:c.336+1412C>T (SEMA4G)	XP_005270065.1:n.336+1412C>T
XM_005270009.3:c.336+1412C>T (SEMA4G)	XP_005270066.1:n.336+1412C>T
XM_005270010.1:c.336+1412C>T (SEMA4G)	XP_005270067.1:n.336+1412C>T
XR_246101.1:n.794+1412C>T (SEMA4G)
XR_945792.1:n.1063+1412C>T (SEMA4G)
XM_024448090.1:c.336+1412C>T (SEMA4G)	XP_024303858.1:n.336+1412C>T
XM_024448091.1:c.336+1412C>T (SEMA4G)	XP_024303859.1:n.336+1412C>T
XR_246101.3:n.794+1412C>T (SEMA4G)
XR_945792.2:n.1042+1412C>T (SEMA4G)
NM_001393925.1:c.336+1412C>T (SEMA4G)	NP_001380854.1:n.336+1412C>T
NM_017893.4:c.336+1412C>T (SEMA4G) MANE Select	NP_060363.2:n.336+1412C>T
NR_172052.1:n.443+1412C>T (SEMA4G)
NR_172053.1:n.443+1412C>T (SEMA4G)
NR_172054.1:n.1041+1412C>T (SEMA4G)
NR_172056.1:n.808+1412C>T (SEMA4G)
NR_172057.1:n.808+1412C>T (SEMA4G)