Canonical Allele Identifier: CA1142006102

Gene: DISP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.223004684T= , CM000663.2:g.223004684T=	GRCh38
NC_000001.10:g.223178026T= , CM000663.1:g.223178026T=	GRCh37
NC_000001.9:g.221244649T=	NCBI36
NG_009243.2:g.194596T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674709.1:c.*2814T=	ENSP00000502092.1:n.*2814T=
ENST00000674736.1:c.*2643T=	ENSP00000501873.1:n.*2643T=
ENST00000675039.1:c.3287T=	ENSP00000501574.1:p.Met1096=
ENST00000675850.1:c.3287T= MANE Select	ENSP00000502357.1:p.Met1096=
ENST00000675961.1:c.3287T=	ENSP00000501808.1:p.Met1096=
ENST00000676139.1:c.*2620T=	ENSP00000502496.1:n.*2620T=
ENST00000284476.7:c.3287T=	ENSP00000284476.6:p.Met1096=
NM_032890.3:c.3287T=	NP_116279.2:p.Met1096=
XM_005273335.1:c.3287T=	XP_005273392.1:p.Met1096=
XM_006711592.1:c.3287T=	XP_006711655.1:p.Met1096=
XM_006711594.2:c.2705T=	XP_006711657.1:p.Met902=
XM_011510072.1:c.3287T=	XP_011508374.1:p.Met1096=
XM_011510073.1:c.3287T=	XP_011508375.1:p.Met1096=
XM_011510074.1:c.3287T=	XP_011508376.1:p.Met1096=
XM_011510075.1:c.3287T=	XP_011508377.1:p.Met1096=
XM_011510076.1:c.3287T=	XP_011508378.1:p.Met1096=
XM_011510077.1:c.3287T=	XP_011508379.1:p.Met1096=
XM_011510078.1:c.2705T=	XP_011508380.1:p.Met902=
NM_001350630.1:c.2558T=	NP_001337559.1:p.Met853=
NM_032890.4:c.3287T=	NP_116279.2:p.Met1096=
XM_005273335.2:c.3287T=	XP_005273392.1:p.Met1096=
XM_006711592.2:c.3287T=	XP_006711655.1:p.Met1096=
XM_006711594.3:c.2705T=	XP_006711657.1:p.Met902=
XM_011510072.2:c.3287T=	XP_011508374.1:p.Met1096=
XM_011510073.2:c.3287T=	XP_011508375.1:p.Met1096=
XM_011510074.2:c.3287T=	XP_011508376.1:p.Met1096=
XM_011510075.2:c.3287T=	XP_011508377.1:p.Met1096=
XM_011510077.2:c.3287T=	XP_011508379.1:p.Met1096=
XM_017002611.1:c.3287T=	XP_016858100.1:p.Met1096=
XM_017002612.1:c.2705T=	XP_016858101.1:p.Met902=
NM_001350630.2:c.2558T=	NP_001337559.1:p.Met853=
NM_001369594.1:c.3287T=	NP_001356523.1:p.Met1096=
NM_001377228.1:c.3287T=	NP_001364157.1:p.Met1096=
NM_001377229.1:c.3287T= MANE Select	NP_001364158.1:p.Met1096=
NM_032890.5:c.3287T=	NP_116279.2:p.Met1096=