Canonical Allele Identifier: CA2209578778

Gene: NTAN1 PDXDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15038251A= , CM000678.2:g.15038251A=	GRCh38
NC_000016.9:g.15132108A= , CM000678.1:g.15132108A=	GRCh37
NC_000016.8:g.15039609A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015027.4:c.*1976A= (PDXDC1) MANE Select	NP_055842.2:n.*1976A=
NM_173474.4:c.754-41T= (NTAN1) MANE Select	NP_775745.1:n.754-41T=
ENST00000287706.8:c.754-41T= (NTAN1) MANE Select	ENSP00000287706.3:n.754-41T=
ENST00000396410.9:c.*1976A= (PDXDC1) MANE Select	ENSP00000379691.4:n.*1976A=
NM_001270766.1:c.439-41T= (NTAN1)	NP_001257695.1:n.439-41T=
NM_001270766.2:c.439-41T= (NTAN1)	NP_001257695.1:n.439-41T=
NM_001270767.1:c.439-41T= (NTAN1)	NP_001257696.1:n.439-41T=
NM_001270767.2:c.439-41T= (NTAN1)	NP_001257696.1:n.439-41T=
NM_001285444.1:c.*1976A= (PDXDC1)	NP_001272373.1:n.*1976A=
NM_001285444.2:c.*1976A= (PDXDC1)	NP_001272373.1:n.*1976A=
NM_001285445.1:c.*1976A= (PDXDC1)	NP_001272374.1:n.*1976A=
NM_001285445.2:c.*1976A= (PDXDC1)	NP_001272374.1:n.*1976A=
NM_001285447.1:c.*1976A= (PDXDC1)	NP_001272376.1:n.*1976A=
NM_001285448.1:c.*1976A= (PDXDC1)	NP_001272377.1:n.*1976A=
NM_001285449.1:c.1399+8195A= (PDXDC1)	NP_001272378.1:n.1399+8195A=
NM_001285449.2:c.1399+8195A= (PDXDC1)	NP_001272378.1:n.1399+8195A=
NM_001324019.1:c.*1976A= (PDXDC1)	NP_001310948.1:n.*1976A=
NM_001324019.2:c.*1976A= (PDXDC1)	NP_001310948.1:n.*1976A=
NM_001324020.1:c.1396+8195A= (PDXDC1)	NP_001310949.1:n.1396+8195A=
NM_001324020.2:c.1396+8195A= (PDXDC1)	NP_001310949.1:n.1396+8195A=
NM_001324021.1:c.1318+8195A= (PDXDC1)	NP_001310950.1:n.1318+8195A=
NM_001324021.2:c.1318+8195A= (PDXDC1)	NP_001310950.1:n.1318+8195A=
NM_015027.3:c.*1976A= (PDXDC1)	NP_055842.2:n.*1976A=
NM_173474.3:c.754-41T= (NTAN1)	NP_775745.1:n.754-41T=
ENST00000287706.7:c.754-41T= (NTAN1)	ENSP00000287706.3:n.754-41T=
ENST00000396410.8:c.*1976A= (PDXDC1)	ENSP00000379691.4:n.*1976A=
ENST00000450288.3:c.*1976A= (PDXDC1)	ENSP00000391147.3:n.*1976A=
ENST00000535621.6:c.1399+8195A= (PDXDC1)	ENSP00000437835.2:n.1399+8195A=
ENST00000565187.5:c.*513-41T= (NTAN1)	ENSP00000457467.1:n.*513-41T=
ENST00000566542.5:n.2042-41T= (NTAN1)
ENST00000568738.1:c.374-41T= (NTAN1)	ENSP00000454595.1:n.374-41T=
ENST00000622833.4:c.439-41T= (NTAN1)	ENSP00000483643.1:n.439-41T=
ENST00000624579.3:c.439-41T= (NTAN1)	ENSP00000485340.1:n.439-41T=
XM_011522355.1:c.505-41T= (NTAN1)	XP_011520657.1:n.505-41T=
XM_011522355.2:c.505-41T= (NTAN1)	XP_011520657.1:n.505-41T=
XM_017023065.1:c.1354+8195A= (PDXDC1)	XP_016878554.1:n.1354+8195A=
XM_024450194.1:c.1354+8195A= (PDXDC1)	XP_024305962.1:n.1354+8195A=
XM_024450195.1:c.1453+8195A= (PDXDC1)	XP_024305963.1:n.1453+8195A=
XM_024450196.1:c.1426+8195A= (PDXDC1)	XP_024305964.1:n.1426+8195A=
XM_024450197.1:c.1273+8195A= (PDXDC1)	XP_024305965.1:n.1273+8195A=