Canonical Allele Identifier: CA3230109
Gene: SPEF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35641517A>G , CM000667.2:g.35641517A>G GRCh38
NC_000005.9:g.35641619A>G , CM000667.1:g.35641619A>G GRCh37
NC_000005.8:g.35677376A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356031.8:c.248A>G MANE Select ENSP00000348314.3:p.His83Arg
ENST00000637569.1:c.248A>G ENSP00000490886.1:p.His83Arg
ENST00000282469.10:c.248A>G ENSP00000282469.6:p.His83Arg
ENST00000356031.7:c.248A>G ENSP00000348314.3:p.His83Arg
ENST00000440995.6:c.248A>G ENSP00000412125.2:p.His83Arg
ENST00000505088.1:n.345A>G
ENST00000505847.5:c.248A>G ENSP00000425448.1:p.His83Arg
ENST00000509059.5:c.248A>G ENSP00000421593.1:p.His83Arg
ENST00000510777.5:c.248A>G ENSP00000426259.1:p.His83Arg
NM_024867.3:c.248A>G NP_079143.3:p.His83Arg
NM_144722.3:c.248A>G NP_653323.1:p.His83Arg
XM_005248376.3:c.248A>G XP_005248433.1:p.His83Arg
XM_005248377.2:c.248A>G XP_005248434.1:p.His83Arg
XM_005248378.2:c.248A>G XP_005248435.1:p.His83Arg
XM_006714501.2:c.248A>G XP_006714564.1:p.His83Arg
XM_011514135.1:c.248A>G XP_011512437.1:p.His83Arg
XM_011514136.1:c.248A>G XP_011512438.1:p.His83Arg
XM_011514137.1:c.248A>G XP_011512439.1:p.His83Arg
XM_011514138.1:c.248A>G XP_011512440.1:p.His83Arg
XM_011514139.1:c.248A>G XP_011512441.1:p.His83Arg
XM_011514140.1:c.248A>G XP_011512442.1:p.His83Arg
XM_011514141.1:c.-374A>G XP_011512443.1:n.-374A>G
XM_011514142.1:c.248A>G XP_011512444.1:p.His83Arg
XR_925655.1:n.464A>G
XR_925656.1:n.463A>G
XM_005248376.4:c.248A>G XP_005248433.1:p.His83Arg
XM_005248377.4:c.248A>G XP_005248434.1:p.His83Arg
XM_005248378.4:c.248A>G XP_005248435.1:p.His83Arg
XM_011514135.3:c.248A>G XP_011512437.1:p.His83Arg
XM_011514136.3:c.248A>G XP_011512438.1:p.His83Arg
XM_011514137.3:c.248A>G XP_011512439.1:p.His83Arg
XM_011514138.3:c.248A>G XP_011512440.1:p.His83Arg
XM_011514139.3:c.248A>G XP_011512441.1:p.His83Arg
XM_011514140.2:c.248A>G XP_011512442.1:p.His83Arg
XM_011514141.3:c.-374A>G XP_011512443.1:n.-374A>G
XM_017009880.2:c.248A>G XP_016865369.1:p.His83Arg
XM_017009881.2:c.-1029A>G XP_016865370.1:n.-1029A>G
XM_017009882.2:c.248A>G XP_016865371.1:p.His83Arg
XM_024446219.1:c.248A>G XP_024301987.1:p.His83Arg
XR_001742273.2:n.351A>G
XR_925655.2:n.351A>G
XR_925656.3:n.351A>G
NM_024867.4:c.248A>G MANE Select NP_079143.3:p.His83Arg
NM_144722.4:c.248A>G NP_653323.1:p.His83Arg