Canonical Allele Identifier: CA3230878

Gene: SPEF2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35708993C>T , CM000667.2:g.35708993C>T	GRCh38
NC_000005.9:g.35709095C>T , CM000667.1:g.35709095C>T	GRCh37
NC_000005.8:g.35744852C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356031.8:c.2711C>T MANE Select	ENSP00000348314.3:p.Ala904Val
ENST00000637569.1:c.2711C>T	ENSP00000490886.1:p.Ala904Val
ENST00000356031.7:c.2711C>T	ENSP00000348314.3:p.Ala904Val
ENST00000440995.6:c.2696C>T	ENSP00000412125.2:p.Ala899Val
ENST00000503074.1:n.4389C>T
ENST00000509059.5:c.2696C>T	ENSP00000421593.1:p.Ala899Val
NM_024867.3:c.2711C>T	NP_079143.3:p.Ala904Val
XM_005248376.3:c.2711C>T	XP_005248433.1:p.Ala904Val
XM_005248377.2:c.2696C>T	XP_005248434.1:p.Ala899Val
XM_005248378.2:c.2711C>T	XP_005248435.1:p.Ala904Val
XM_006714501.2:c.2711C>T	XP_006714564.1:p.Ala904Val
XM_011514135.1:c.2711C>T	XP_011512437.1:p.Ala904Val
XM_011514136.1:c.2711C>T	XP_011512438.1:p.Ala904Val
XM_011514137.1:c.2696C>T	XP_011512439.1:p.Ala899Val
XM_011514138.1:c.2711C>T	XP_011512440.1:p.Ala904Val
XM_011514139.1:c.2711C>T	XP_011512441.1:p.Ala904Val
XM_011514140.1:c.2540C>T	XP_011512442.1:p.Ala847Val
XM_011514141.1:c.2285C>T	XP_011512443.1:p.Ala762Val
XM_011514142.1:c.2711C>T	XP_011512444.1:p.Ala904Val
XR_925655.1:n.2927C>T
XR_925656.1:n.2926C>T
XM_005248376.4:c.2711C>T	XP_005248433.1:p.Ala904Val
XM_005248377.4:c.2696C>T	XP_005248434.1:p.Ala899Val
XM_005248378.4:c.2711C>T	XP_005248435.1:p.Ala904Val
XM_011514135.3:c.2711C>T	XP_011512437.1:p.Ala904Val
XM_011514136.3:c.2711C>T	XP_011512438.1:p.Ala904Val
XM_011514137.3:c.2696C>T	XP_011512439.1:p.Ala899Val
XM_011514138.3:c.2711C>T	XP_011512440.1:p.Ala904Val
XM_011514139.3:c.2711C>T	XP_011512441.1:p.Ala904Val
XM_011514140.2:c.2540C>T	XP_011512442.1:p.Ala847Val
XM_011514141.3:c.2285C>T	XP_011512443.1:p.Ala762Val
XM_017009880.2:c.2525C>T	XP_016865369.1:p.Ala842Val
XM_017009881.2:c.2285C>T	XP_016865370.1:p.Ala762Val
XM_017009882.2:c.2711C>T	XP_016865371.1:p.Ala904Val
XM_024446219.1:c.2540C>T	XP_024301987.1:p.Ala847Val
XR_001742273.2:n.2814C>T
XR_001742634.1:n.1704-10958G>A
XR_001742635.1:n.1601-10958G>A
XR_001742636.1:n.1791-10958G>A
XR_925655.2:n.2814C>T
XR_925656.3:n.2814C>T
NM_024867.4:c.2711C>T MANE Select	NP_079143.3:p.Ala904Val