Canonical Allele Identifier: CA11920338
Gene: SEMA5A HGNC NCBI

Linked Data

dbSNP Id: rs7702187
gnomAD v2: 5-9332281-T-A
gnomAD v3: 5-9332169-T-A
gnomAD v4: 5-9332169-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.9332169T>A , CM000667.2:g.9332169T>A GRCh38
NC_000005.9:g.9332281T>A , CM000667.1:g.9332281T>A GRCh37
NC_000005.8:g.9385281T>A NCBI36
NG_016410.1:g.218953A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382496.10:c.224+5544A>T MANE Select ENSP00000371936.5:n.224+5544A>T
ENST00000652226.1:c.224+5544A>T ENSP00000499013.1:n.224+5544A>T
ENST00000382496.9:c.224+5544A>T ENSP00000371936.5:n.224+5544A>T
ENST00000509486.2:n.301+5544A>T
ENST00000513968.4:c.224+5544A>T ENSP00000421961.1:n.224+5544A>T
NM_003966.2:c.224+5544A>T NP_003957.2:n.224+5544A>T
XM_006714506.2:c.224+5544A>T XP_006714569.1:n.224+5544A>T
XM_006714507.2:c.224+5544A>T XP_006714570.1:n.224+5544A>T
XM_011514155.1:c.224+5544A>T XP_011512457.1:n.224+5544A>T
XM_011514156.1:c.224+5544A>T XP_011512458.1:n.224+5544A>T
XM_011514157.1:c.224+5544A>T XP_011512459.1:n.224+5544A>T
XM_011514158.1:c.224+5544A>T XP_011512460.1:n.224+5544A>T
XM_006714506.3:c.224+5544A>T XP_006714569.1:n.224+5544A>T
XM_006714507.3:c.224+5544A>T XP_006714570.1:n.224+5544A>T
XM_011514155.2:c.224+5544A>T XP_011512457.1:n.224+5544A>T
XM_011514156.2:c.224+5544A>T XP_011512458.1:n.224+5544A>T
XM_011514157.2:c.224+5544A>T XP_011512459.1:n.224+5544A>T
XM_011514158.2:c.224+5544A>T XP_011512460.1:n.224+5544A>T
XM_017010016.2:c.-247-13752A>T XP_016865505.1:n.-247-13752A>T
NM_003966.3:c.224+5544A>T MANE Select NP_003957.2:n.224+5544A>T