Canonical Allele Identifier: CA4997442

Gene: CNTLN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.17409337T>C , CM000671.2:g.17409337T>C	GRCh38
NC_000009.11:g.17409335T>C , CM000671.1:g.17409335T>C	GRCh37
NC_000009.10:g.17399335T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017738.4:c.2660T>C MANE Select	NP_060208.2:p.Ile887Thr
ENST00000380647.8:c.2660T>C MANE Select	ENSP00000370021.3:p.Ile887Thr
NM_001365029.1:c.2657T>C	NP_001351958.1:p.Ile886Thr
NM_017738.3:c.2660T>C	NP_060208.2:p.Ile887Thr
ENST00000380647.7:c.2660T>C	ENSP00000370021.3:p.Ile887Thr
XM_005251492.1:c.2657T>C	XP_005251549.1:p.Ile886Thr
XM_006716793.2:c.2471T>C	XP_006716856.1:p.Ile824Thr
XM_006716793.4:c.2471T>C	XP_006716856.1:p.Ile824Thr
XM_011517940.1:c.2660T>C	XP_011516242.1:p.Ile887Thr
XM_011517941.1:c.2660T>C	XP_011516243.1:p.Ile887Thr
XM_011517941.2:c.2660T>C	XP_011516243.1:p.Ile887Thr
XM_011517942.1:c.833T>C	XP_011516244.1:p.Ile278Thr
XM_017014839.1:c.2660T>C	XP_016870328.1:p.Ile887Thr
XM_017014840.2:c.2660T>C	XP_016870329.1:p.Ile887Thr
XM_017014841.1:c.2465T>C	XP_016870330.1:p.Ile822Thr
XM_017014842.1:c.2660T>C	XP_016870331.1:p.Ile887Thr
XM_017014843.1:c.2660T>C	XP_016870332.1:p.Ile887Thr
XM_017014844.1:c.1280T>C	XP_016870333.1:p.Ile427Thr
XM_017014845.2:c.959T>C	XP_016870334.1:p.Ile320Thr
XM_017014846.1:c.605T>C	XP_016870335.1:p.Ile202Thr
XM_017014847.2:c.605T>C	XP_016870336.1:p.Ile202Thr
XM_024447583.1:c.2660T>C	XP_024303351.1:p.Ile887Thr
XR_929281.1:n.2735T>C
XR_929282.1:n.2735T>C
XR_929282.2:n.2735T>C