Canonical Allele Identifier: CA3194830989

Gene: TPCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.113288122T= , CM000674.2:g.113288122T=	GRCh38
NC_000012.11:g.113725927T= , CM000674.1:g.113725927T=	GRCh37
NC_000012.10:g.112210310T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017901.6:c.1635-41T= MANE Select	NP_060371.2:n.1635-41T=
ENST00000335509.11:c.1635-41T= MANE Select	ENSP00000335300.6:n.1635-41T=
NM_001143819.2:c.1851-41T=	NP_001137291.1:n.1851-41T=
NM_001143819.3:c.1851-41T=	NP_001137291.1:n.1851-41T=
NM_001301214.1:c.1431-41T=	NP_001288143.1:n.1431-41T=
NM_001301214.2:c.1431-41T=	NP_001288143.1:n.1431-41T=
NM_001351346.1:c.1431-41T=	NP_001338275.1:n.1431-41T=
NM_001351346.2:c.1431-41T=	NP_001338275.1:n.1431-41T=
NM_001351347.1:c.1431-41T=	NP_001338276.1:n.1431-41T=
NM_017901.5:c.1635-41T=	NP_060371.2:n.1635-41T=
ENST00000335509.10:c.1635-41T=	ENSP00000335300.6:n.1635-41T=
ENST00000392569.8:c.1431-41T=	ENSP00000376350.4:n.1431-41T=
ENST00000428632.7:n.1764-41T=
ENST00000541517.5:c.1851-41T=	ENSP00000438125.1:n.1851-41T=
ENST00000547955.5:c.238-41T=
ENST00000550785.5:c.1851-41T=	ENSP00000448083.1:n.1851-41T=
ENST00000551127.5:n.609-41T=
ENST00000552077.5:n.1901-41T=
XM_005253905.2:c.1839-41T=	XP_005253962.2:n.1839-41T=
XM_005253906.3:c.1431-41T=	XP_005253963.1:n.1431-41T=
XM_011538489.1:c.1893-41T=	XP_011536791.1:n.1893-41T=
XM_011538490.1:c.1851-41T=	XP_011536792.1:n.1851-41T=
XM_011538490.2:c.1851-41T=	XP_011536792.1:n.1851-41T=
XM_011538492.1:c.1635-41T=	XP_011536794.1:n.1635-41T=
XM_011538492.2:c.1635-41T=	XP_011536794.1:n.1635-41T=
XM_011538493.1:c.1431-41T=	XP_011536795.1:n.1431-41T=
XM_011538493.2:c.1431-41T=	XP_011536795.1:n.1431-41T=
XM_011538494.1:c.1431-41T=	XP_011536796.1:n.1431-41T=
XM_017019480.2:c.1797-41T=	XP_016874969.1:n.1797-41T=
XM_017019482.2:c.1851-41T=	XP_016874971.1:n.1851-41T=
XR_001748765.2:n.2020-41T=
XR_001748766.2:n.2020-41T=
XR_001748767.2:n.2020-41T=
XR_243017.2:n.2010-41T=