Canonical Allele Identifier: CA1836699754

Gene: CNTLN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.17487947T= , CM000671.2:g.17487947T=	GRCh38
NC_000009.11:g.17487945T= , CM000671.1:g.17487945T=	GRCh37
NC_000009.10:g.17477945T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380647.8:c.4119+881T= MANE Select	ENSP00000370021.3:n.4119+881T=
ENST00000380647.7:c.4119+881T=	ENSP00000370021.3:n.4119+881T=
NM_017738.3:c.4119+881T=	NP_060208.2:n.4119+881T=
XM_005251492.1:c.4116+881T=	XP_005251549.1:n.4116+881T=
XM_006716793.2:c.3930+881T=	XP_006716856.1:n.3930+881T=
XM_011517940.1:c.4119+881T=	XP_011516242.1:n.4119+881T=
XM_011517942.1:c.2292+881T=	XP_011516244.1:n.2292+881T=
NM_001365029.1:c.4116+881T=	NP_001351958.1:n.4116+881T=
XM_006716793.4:c.3930+881T=	XP_006716856.1:n.3930+881T=
XM_017014839.1:c.4119+881T=	XP_016870328.1:n.4119+881T=
XM_017014840.2:c.4119+881T=	XP_016870329.1:n.4119+881T=
XM_017014841.1:c.3924+881T=	XP_016870330.1:n.3924+881T=
XM_017014844.1:c.2739+881T=	XP_016870333.1:n.2739+881T=
XM_017014845.2:c.2418+881T=	XP_016870334.1:n.2418+881T=
XM_017014846.1:c.2064+881T=	XP_016870335.1:n.2064+881T=
XM_017014847.2:c.2064+881T=	XP_016870336.1:n.2064+881T=
NM_017738.4:c.4119+881T= MANE Select	NP_060208.2:n.4119+881T=