Canonical Allele Identifier: CA1155134

Gene: SEMA4A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156160931C>T , CM000663.2:g.156160931C>T	GRCh38
NC_000001.10:g.156130722C>T , CM000663.1:g.156130722C>T	GRCh37
NC_000001.9:g.154397346C>T	NCBI36
NG_027683.1:g.15988C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022367.4:c.712C>T MANE Select	NP_071762.2:p.Pro238Ser
ENST00000368285.8:c.712C>T MANE Select	ENSP00000357268.3:p.Pro238Ser
NM_001193300.1:c.712C>T	NP_001180229.1:p.Pro238Ser
NM_001193300.2:c.712C>T	NP_001180229.1:p.Pro238Ser
NM_001193301.1:c.712C>T	NP_001180230.1:p.Pro238Ser
NM_001193301.2:c.712C>T	NP_001180230.1:p.Pro238Ser
NM_001193302.1:c.316C>T	NP_001180231.1:p.Pro106Ser
NM_001193302.2:c.316C>T	NP_001180231.1:p.Pro106Ser
NM_001370567.1:c.712C>T	NP_001357496.1:p.Pro238Ser
NM_001370568.1:c.415C>T	NP_001357497.1:p.Pro139Ser
NM_001370569.1:c.205C>T	NP_001357498.1:p.Pro69Ser
NM_001370571.1:c.205C>T	NP_001357500.1:p.Pro69Ser
NM_022367.3:c.712C>T	NP_071762.2:p.Pro238Ser
ENST00000355014.6:c.712C>T	ENSP00000347117.2:p.Pro238Ser
ENST00000368282.1:c.712C>T	ENSP00000357265.1:p.Pro238Ser
ENST00000368284.5:c.316C>T	ENSP00000357267.1:p.Pro106Ser
ENST00000368285.7:c.712C>T	ENSP00000357268.3:p.Pro238Ser
ENST00000368286.6:c.598C>T	ENSP00000357269.3:p.Pro200Ser
ENST00000414683.5:c.415C>T	ENSP00000399230.1:p.Pro139Ser
ENST00000435124.5:c.712C>T	ENSP00000401391.1:p.Pro238Ser
ENST00000438830.5:c.613C>T	ENSP00000392865.1:p.Pro205Ser
ENST00000466698.1:n.43C>T
ENST00000487358.5:n.609C>T
XM_011509871.1:c.598C>T	XP_011508173.1:p.Pro200Ser
XM_011509871.3:c.598C>T	XP_011508173.1:p.Pro200Ser
XM_011509872.1:c.712C>T	XP_011508174.1:p.Pro238Ser
XM_011509872.2:c.712C>T	XP_011508174.1:p.Pro238Ser
XM_011509873.1:c.712C>T	XP_011508175.1:p.Pro238Ser
XM_011509873.2:c.712C>T	XP_011508175.1:p.Pro238Ser
XM_011509874.1:c.415C>T	XP_011508176.1:p.Pro139Ser
XM_011509874.2:c.415C>T	XP_011508176.1:p.Pro139Ser
XM_011509875.1:c.415C>T	XP_011508177.1:p.Pro139Ser
XM_011509875.3:c.415C>T	XP_011508177.1:p.Pro139Ser
XM_011509876.1:c.415C>T	XP_011508178.1:p.Pro139Ser
XM_011509876.2:c.415C>T	XP_011508178.1:p.Pro139Ser
XM_011509877.1:c.415C>T	XP_011508179.1:p.Pro139Ser
XM_011509878.1:c.415C>T	XP_011508180.1:p.Pro139Ser
XM_011509878.2:c.415C>T	XP_011508180.1:p.Pro139Ser
XM_011509879.1:c.205C>T	XP_011508181.1:p.Pro69Ser
XM_011509879.2:c.205C>T	XP_011508181.1:p.Pro69Ser
XM_017002056.1:c.712C>T	XP_016857545.1:p.Pro238Ser
XM_017002057.1:c.205C>T	XP_016857546.1:p.Pro69Ser