Canonical Allele Identifier: CA1398209831
Gene: SEMA5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123019401G= , CM000665.2:g.123019401G= GRCh38
NC_000003.11:g.122738248G= , CM000665.1:g.122738248G= GRCh37
NC_000003.10:g.124220938G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357599.8:c.-39+8063C= MANE Select ENSP00000350215.3:n.-39+8063C=
ENST00000648990.1:c.-51+8063C= ENSP00000497595.1:n.-51+8063C=
ENST00000649167.1:n.248+8063C=
ENST00000195173.8:c.-51+8063C= ENSP00000195173.5:n.-51+8063C=
ENST00000357599.7:c.-39+8063C= ENSP00000350215.3:n.-39+8063C=
ENST00000421053.5:c.-39+7697C= ENSP00000401056.1:n.-39+7697C=
ENST00000465147.1:n.303+8063C=
ENST00000475244.5:c.-39+9046C= ENSP00000417570.1:n.-39+9046C=
ENST00000477001.1:n.115+8063C=
NM_001031702.3:c.-39+8063C= NP_001026872.2:n.-39+8063C=
NM_001256348.1:c.-51+8063C= NP_001243277.1:n.-51+8063C=
NR_046079.1:n.159+9046C=
XM_011512918.1:c.-51+8063C= XP_011511220.1:n.-51+8063C=
XR_924407.1:n.12-2611G=
XM_017006639.1:c.-51+8063C= XP_016862128.1:n.-51+8063C=
NM_001031702.4:c.-39+8063C= MANE Select NP_001026872.2:n.-39+8063C=
NM_001256348.2:c.-51+8063C= NP_001243277.1:n.-51+8063C=
NR_046079.2:n.159+9046C=