Canonical Allele Identifier: CA1657098129

Gene: NT5DC1 COL10A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116130951G= , CM000668.2:g.116130951G=	GRCh38
NC_000006.11:g.116452114G= , CM000668.1:g.116452114G=	GRCh37
NC_000006.10:g.116558807G=	NCBI36
NG_008032.1:g.183C=
NG_021351.1:g.35116G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000319550.9:c.529+13006G= (NT5DC1) MANE Select	ENSP00000326858.3:n.529+13006G=
ENST00000319550.8:c.529+13006G= (NT5DC1)	ENSP00000326858.3:n.529+13006G=
ENST00000418500.1:c.-15-5444C= (COL10A1)	ENSP00000392712.1:n.-15-5444C=
ENST00000419791.3:c.529+13006G= (NT5DC1)	ENSP00000393578.1:n.529+13006G=
ENST00000460749.1:c.27+13006G= (NT5DC1)
NM_152729.2:c.529+13006G= (NT5DC1)	NP_689942.2:n.529+13006G=
XM_006715333.2:c.-15-5444C= (COL10A1)	XP_006715396.1:n.-15-5444C=
XM_006715377.2:c.529+13006G= (NT5DC1)	XP_006715440.1:n.529+13006G=
XM_006715378.2:c.529+13006G= (NT5DC1)	XP_006715441.1:n.529+13006G=
XM_011535432.1:c.-15-5444C= (COL10A1)	XP_011533734.1:n.-15-5444C=
XM_011535433.1:c.-15-5444C= (COL10A1)	XP_011533735.1:n.-15-5444C=
XM_006715333.3:c.-15-5444C= (COL10A1)	XP_006715396.1:n.-15-5444C=
XM_006715378.3:c.529+13006G= (NT5DC1)	XP_006715441.1:n.529+13006G=
XM_011535432.3:c.-15-5444C= (COL10A1)	XP_011533734.1:n.-15-5444C=
XM_011535433.3:c.-15-5444C= (COL10A1)	XP_011533735.1:n.-15-5444C=
NM_152729.3:c.529+13006G= (NT5DC1) MANE Select	NP_689942.2:n.529+13006G=