Canonical Allele Identifier: CA465638687

Gene: SEMA4D

Linked Data

• MyVariant Identifiers: chr9:g.92003587G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.89388672G>A , CM000671.2:g.89388672G>A	GRCh38
NC_000009.11:g.92003587G>A , CM000671.1:g.92003587G>A	GRCh37
NC_000009.10:g.91193407G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000422704.7:c.1071C>T MANE Select	ENSP00000388768.2:p.Arg357=
ENST00000339861.8:c.1071C>T	ENSP00000344923.4:p.Arg357=
ENST00000356444.6:c.1071C>T	ENSP00000348822.2:p.Arg357=
ENST00000420987.5:c.1071C>T	ENSP00000391733.1:p.Arg357=
ENST00000422704.6:c.1071C>T	ENSP00000388768.2:p.Arg357=
ENST00000429836.5:c.1071C>T	ENSP00000395222.1:p.Arg357=
ENST00000438547.6:c.1071C>T	ENSP00000405102.2:p.Arg357=
ENST00000450295.5:c.1071C>T	ENSP00000416523.1:p.Arg357=
ENST00000455551.6:c.1071C>T	ENSP00000411981.2:p.Arg357=
ENST00000474258.1:n.55C>T
ENST00000537934.5:c.1071C>T	ENSP00000446394.1:p.Arg357=
NM_001142287.1:c.1071C>T	NP_001135759.1:p.Arg357=
NM_006378.3:c.1071C>T	NP_006369.3:p.Arg357=
XM_005251654.2:c.1071C>T	XP_005251711.1:p.Arg357=
XM_011518123.1:c.1071C>T	XP_011516425.1:p.Arg357=
XM_011518124.1:c.1071C>T	XP_011516426.1:p.Arg357=
XM_011518125.1:c.1071C>T	XP_011516427.1:p.Arg357=
XM_011518126.1:c.1071C>T	XP_011516428.1:p.Arg357=
XM_011518127.1:c.1071C>T	XP_011516429.1:p.Arg357=
XM_011518128.1:c.1071C>T	XP_011516430.1:p.Arg357=
XM_011518129.1:c.1071C>T	XP_011516431.1:p.Arg357=
XM_011518130.1:c.1071C>T	XP_011516432.1:p.Arg357=
XM_011518131.1:c.1071C>T	XP_011516433.1:p.Arg357=
XM_011518132.1:c.1071C>T	XP_011516434.1:p.Arg357=
XM_011518133.1:c.1071C>T	XP_011516435.1:p.Arg357=
XM_011518134.1:c.1071C>T	XP_011516436.1:p.Arg357=
XM_011518135.1:c.1071C>T	XP_011516437.1:p.Arg357=
XM_011518136.1:c.1071C>T	XP_011516438.1:p.Arg357=
XM_011518137.1:c.1071C>T	XP_011516439.1:p.Arg357=
XR_242562.2:n.1837C>T
XR_929702.1:n.1743C>T
XM_005251654.3:c.1071C>T	XP_005251711.1:p.Arg357=
XM_011518123.2:c.1071C>T	XP_011516425.1:p.Arg357=
XM_011518124.2:c.1071C>T	XP_011516426.1:p.Arg357=
XM_011518127.2:c.1071C>T	XP_011516429.1:p.Arg357=
XM_011518128.2:c.1071C>T	XP_011516430.1:p.Arg357=
XM_011518130.2:c.1071C>T	XP_011516432.1:p.Arg357=
XM_011518131.2:c.1071C>T	XP_011516433.1:p.Arg357=
XM_011518133.2:c.1071C>T	XP_011516435.1:p.Arg357=
XM_011518134.2:c.1071C>T	XP_011516436.1:p.Arg357=
XM_017014193.2:c.1071C>T	XP_016869682.1:p.Arg357=
XM_017014194.1:c.1071C>T	XP_016869683.1:p.Arg357=
XM_017014195.1:c.1071C>T	XP_016869684.1:p.Arg357=
XM_017014196.1:c.1071C>T	XP_016869685.1:p.Arg357=
XM_017014197.1:c.1071C>T	XP_016869686.1:p.Arg357=
XM_017014198.1:c.1071C>T	XP_016869687.1:p.Arg357=
XM_017014199.1:c.1071C>T	XP_016869688.1:p.Arg357=
XR_001746153.1:n.1687C>T
XR_001746154.1:n.1769C>T
XR_001746155.1:n.1810C>T
XR_001746156.1:n.1666C>T
XR_001746157.1:n.1706C>T
XR_001746158.1:n.1747C>T
XR_242562.4:n.1837C>T
NM_001142287.2:c.1071C>T	NP_001135759.1:p.Arg357=
NM_001371194.2:c.1071C>T MANE Select	NP_001358123.1:p.Arg357=
NM_001371195.1:c.1071C>T	NP_001358124.1:p.Arg357=
NM_001371196.1:c.1071C>T	NP_001358125.1:p.Arg357=
NM_001371197.1:c.1071C>T	NP_001358126.1:p.Arg357=
NM_001371198.1:c.1071C>T	NP_001358127.1:p.Arg357=
NM_001371199.1:c.1071C>T	NP_001358128.1:p.Arg357=
NM_001371200.1:c.1071C>T	NP_001358129.1:p.Arg357=
NM_001371201.1:c.1071C>T	NP_001358130.1:p.Arg357=
NM_001371202.1:c.1071C>T	NP_001358131.1:p.Arg357=
NM_006378.4:c.1071C>T	NP_006369.3:p.Arg357=
NR_163884.1:n.1762C>T
NR_163885.1:n.1810C>T
NR_163886.1:n.1699C>T
NR_163887.1:n.1747C>T
NR_163888.1:n.1837C>T
NR_163889.1:n.1699C>T