Canonical Allele Identifier: CA1398209821

Gene: SEMA5B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123019371A= , CM000665.2:g.123019371A=	GRCh38
NC_000003.11:g.122738218A= , CM000665.1:g.122738218A=	GRCh37
NC_000003.10:g.124220908A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357599.8:c.-39+8093T= MANE Select	ENSP00000350215.3:n.-39+8093T=
ENST00000648990.1:c.-51+8093T=	ENSP00000497595.1:n.-51+8093T=
ENST00000649167.1:n.248+8093T=
ENST00000195173.8:c.-51+8093T=	ENSP00000195173.5:n.-51+8093T=
ENST00000357599.7:c.-39+8093T=	ENSP00000350215.3:n.-39+8093T=
ENST00000421053.5:c.-39+7727T=	ENSP00000401056.1:n.-39+7727T=
ENST00000465147.1:n.303+8093T=
ENST00000475244.5:c.-39+9076T=	ENSP00000417570.1:n.-39+9076T=
ENST00000477001.1:n.115+8093T=
NM_001031702.3:c.-39+8093T=	NP_001026872.2:n.-39+8093T=
NM_001256348.1:c.-51+8093T=	NP_001243277.1:n.-51+8093T=
NR_046079.1:n.159+9076T=
XM_011512918.1:c.-51+8093T=	XP_011511220.1:n.-51+8093T=
XR_924407.1:n.12-2641A=
XM_017006639.1:c.-51+8093T=	XP_016862128.1:n.-51+8093T=
NM_001031702.4:c.-39+8093T= MANE Select	NP_001026872.2:n.-39+8093T=
NM_001256348.2:c.-51+8093T=	NP_001243277.1:n.-51+8093T=
NR_046079.2:n.159+9076T=