Canonical Allele Identifier: CA1143538411

Gene: SEMA4A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156162993G= , CM000663.2:g.156162993G=	GRCh38
NC_000001.10:g.156132784G= , CM000663.1:g.156132784G=	GRCh37
NC_000001.9:g.154399408G=	NCBI36
NG_027683.1:g.18050G=

Transcript Alleles

HGVS	Amino-acid Change
NM_022367.4:c.1033G= MANE Select	NP_071762.2:p.Asp345=
ENST00000368285.8:c.1033G= MANE Select	ENSP00000357268.3:p.Asp345=
NM_001193300.1:c.1033G=	NP_001180229.1:p.Asp345=
NM_001193300.2:c.1033G=	NP_001180229.1:p.Asp345=
NM_001193301.1:c.1033G=	NP_001180230.1:p.Asp345=
NM_001193301.2:c.1033G=	NP_001180230.1:p.Asp345=
NM_001193302.1:c.637G=	NP_001180231.1:p.Asp213=
NM_001193302.2:c.637G=	NP_001180231.1:p.Asp213=
NM_001370567.1:c.1033G=	NP_001357496.1:p.Asp345=
NM_001370568.1:c.736G=	NP_001357497.1:p.Asp246=
NM_001370569.1:c.526G=	NP_001357498.1:p.Asp176=
NM_001370571.1:c.526G=	NP_001357500.1:p.Asp176=
NM_022367.3:c.1033G=	NP_071762.2:p.Asp345=
ENST00000355014.6:c.1033G=	ENSP00000347117.2:p.Asp345=
ENST00000368282.1:c.1033G=	ENSP00000357265.1:p.Asp345=
ENST00000368284.5:c.637G=	ENSP00000357267.1:p.Asp213=
ENST00000368285.7:c.1033G=	ENSP00000357268.3:p.Asp345=
ENST00000368286.6:c.919G=	ENSP00000357269.3:p.Asp307=
ENST00000462892.1:n.342G=
ENST00000469065.1:n.303G=
ENST00000487358.5:n.930G=
XM_011509871.1:c.919G=	XP_011508173.1:p.Asp307=
XM_011509871.3:c.919G=	XP_011508173.1:p.Asp307=
XM_011509872.1:c.1033G=	XP_011508174.1:p.Asp345=
XM_011509872.2:c.1033G=	XP_011508174.1:p.Asp345=
XM_011509873.1:c.1033G=	XP_011508175.1:p.Asp345=
XM_011509873.2:c.1033G=	XP_011508175.1:p.Asp345=
XM_011509874.1:c.736G=	XP_011508176.1:p.Asp246=
XM_011509874.2:c.736G=	XP_011508176.1:p.Asp246=
XM_011509875.1:c.736G=	XP_011508177.1:p.Asp246=
XM_011509875.3:c.736G=	XP_011508177.1:p.Asp246=
XM_011509876.1:c.736G=	XP_011508178.1:p.Asp246=
XM_011509876.2:c.736G=	XP_011508178.1:p.Asp246=
XM_011509877.1:c.736G=	XP_011508179.1:p.Asp246=
XM_011509878.1:c.736G=	XP_011508180.1:p.Asp246=
XM_011509878.2:c.736G=	XP_011508180.1:p.Asp246=
XM_011509879.1:c.526G=	XP_011508181.1:p.Asp176=
XM_011509879.2:c.526G=	XP_011508181.1:p.Asp176=
XM_017002056.1:c.1033G=	XP_016857545.1:p.Asp345=
XM_017002057.1:c.526G=	XP_016857546.1:p.Asp176=