Canonical Allele Identifier: CA2635387965

Gene: CTNS

Linked Data

• gnomAD v4: 17-3636605-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3636605G>T , CM000679.2:g.3636605G>T	GRCh38
NC_000017.10:g.3539899G>T , CM000679.1:g.3539899G>T	GRCh37
NC_000017.9:g.3486648G>T	NCBI36
NG_012489.1:g.5138G>T
NG_052852.1:g.4718C>A
NG_012489.2:g.5138G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381870.8:c.-333G>T	ENSP00000371294.3:n.-333G>T
ENST00000673965.1:c.-328G>T	ENSP00000500995.1:n.-328G>T
ENST00000046640.7:c.-456G>T	ENSP00000046640.3:n.-456G>T
ENST00000381870.7:c.-333G>T	ENSP00000371294.3:n.-333G>T
NM_001031681.2:c.-333G>T	NP_001026851.2:n.-333G>T
NM_004937.2:c.-456G>T	NP_004928.2:n.-456G>T
XM_005256485.1:c.-456G>T	XP_005256542.1:n.-456G>T
XM_006721463.1:c.-328G>T	XP_006721526.1:n.-328G>T
XM_006721464.1:c.-812G>T	XP_006721527.1:n.-812G>T
XM_011523692.1:c.-817G>T	XP_011521994.1:n.-817G>T
XR_934003.1:n.138G>T
XM_005256485.3:c.-456G>T	XP_005256542.1:n.-456G>T
XM_006721463.3:c.-328G>T	XP_006721526.1:n.-328G>T
XM_006721464.2:c.-812G>T	XP_006721527.1:n.-812G>T
XM_011523692.2:c.-817G>T	XP_011521994.1:n.-817G>T
XM_017024254.1:c.-733G>T	XP_016879743.1:n.-733G>T
XM_017024255.1:c.-812G>T	XP_016879744.1:n.-812G>T
XM_017024256.1:c.-817G>T	XP_016879745.1:n.-817G>T
XM_017024257.1:c.-733G>T	XP_016879746.1:n.-733G>T
XM_017024258.1:c.-732G>T	XP_016879747.1:n.-732G>T
NM_001031681.3:c.-333G>T	NP_001026851.2:n.-333G>T