Canonical Allele Identifier: CA4268630

Gene: PSPH

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.56015152A>G , CM000669.2:g.56015152A>G	GRCh38
NC_000007.13:g.56082845A>G , CM000669.1:g.56082845A>G	GRCh37
NC_000007.12:g.56050339A>G	NCBI36
NG_011473.1:g.41424T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004577.4:c.441T>C MANE Select	NP_004568.2:p.Asp147=
ENST00000275605.8:c.441T>C MANE Select	ENSP00000275605.3:p.Asp147=
NM_001370503.1:c.441T>C	NP_001357432.1:p.Asp147=
NM_001370504.1:c.441T>C	NP_001357433.1:p.Asp147=
NM_001370505.1:c.441T>C	NP_001357434.1:p.Asp147=
NM_001370506.1:c.441T>C	NP_001357435.1:p.Asp147=
NM_001370507.1:c.441T>C	NP_001357436.1:p.Asp147=
NM_001370508.1:c.441T>C	NP_001357437.1:p.Asp147=
NM_001370509.1:c.441T>C	NP_001357438.1:p.Asp147=
NM_001370510.1:c.441T>C	NP_001357439.1:p.Asp147=
NM_001370511.1:c.441T>C	NP_001357440.1:p.Asp147=
NM_001370512.1:c.441T>C	NP_001357441.1:p.Asp147=
NM_001370513.1:c.441T>C	NP_001357442.1:p.Asp147=
NM_001370514.1:c.441T>C	NP_001357443.1:p.Asp147=
NM_001370515.1:c.441T>C	NP_001357444.1:p.Asp147=
NM_001370516.1:c.441T>C	NP_001357445.1:p.Asp147=
NM_001370517.1:c.441T>C	NP_001357446.1:p.Asp147=
NM_001370518.1:c.441T>C	NP_001357447.1:p.Asp147=
NM_001370519.1:c.441T>C	NP_001357448.1:p.Asp147=
NM_001370520.1:c.441T>C	NP_001357449.1:p.Asp147=
NM_001370521.1:c.441T>C	NP_001357450.1:p.Asp147=
NM_001370522.1:c.441T>C	NP_001357451.1:p.Asp147=
NM_004577.3:c.441T>C	NP_004568.2:p.Asp147=
ENST00000275605.7:c.441T>C	ENSP00000275605.3:p.Asp147=
ENST00000395471.7:c.441T>C	ENSP00000378854.3:p.Asp147=
ENST00000421626.5:c.441T>C	ENSP00000398653.1:p.Asp147=
ENST00000437355.6:c.441T>C	ENSP00000401639.2:p.Asp147=
ENST00000459834.5:n.231T>C
XM_005271773.1:c.441T>C	XP_005271830.1:p.Asp147=
XM_005271773.2:c.441T>C	XP_005271830.1:p.Asp147=
XM_005271774.1:c.441T>C	XP_005271831.1:p.Asp147=
XM_005271774.2:c.441T>C	XP_005271831.1:p.Asp147=
XM_005271775.1:c.441T>C	XP_005271832.1:p.Asp147=
XM_005271775.2:c.441T>C	XP_005271832.1:p.Asp147=
XM_005271776.1:c.441T>C	XP_005271833.1:p.Asp147=
XM_005271776.2:c.441T>C	XP_005271833.1:p.Asp147=
XM_006715760.1:c.441T>C	XP_006715823.1:p.Asp147=
XM_006715760.2:c.441T>C	XP_006715823.1:p.Asp147=
XM_006715761.1:c.306T>C	XP_006715824.1:p.Asp102=
XM_006715761.2:c.306T>C	XP_006715824.1:p.Asp102=
XM_011515459.1:c.441T>C	XP_011513761.1:p.Asp147=
XM_011515460.1:c.441T>C	XP_011513762.1:p.Asp147=
XM_011515461.1:c.441T>C	XP_011513763.1:p.Asp147=
XM_011515461.2:c.441T>C	XP_011513763.1:p.Asp147=
XM_011515462.1:c.302T>C	XP_011513764.1:p.Met101Thr
XM_017012466.2:c.441T>C	XP_016867955.1:p.Asp147=
XM_017012467.2:c.441T>C	XP_016867956.1:p.Asp147=
XM_017012468.2:c.306T>C	XP_016867957.1:p.Asp102=
XM_017012469.2:c.306T>C	XP_016867958.1:p.Asp102=
XR_002956470.1:n.1099T>C