Canonical Allele Identifier: CA344742572

Gene: DISP1

Linked Data

• dbSNP Id: rs2789975
• MyVariant Identifiers: chr1:g.223116474G>C (hg19) ; chr1:g.222943132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222943132G>C , CM000663.2:g.222943132G>C	GRCh38
NC_000001.10:g.223116474G>C , CM000663.1:g.223116474G>C	GRCh37
NC_000001.9:g.221183097G>C	NCBI36
NG_009243.2:g.133044G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495684.2:n.163-39948G>C
ENST00000674709.1:c.147+162G>C	ENSP00000502092.1:n.147+162G>C
ENST00000674736.1:c.147+162G>C	ENSP00000501873.1:n.147+162G>C
ENST00000675039.1:c.309G>C	ENSP00000501574.1:p.Glu103Asp
ENST00000675850.1:c.309G>C MANE Select	ENSP00000502357.1:p.Glu103Asp
ENST00000675961.1:c.309G>C	ENSP00000501808.1:p.Glu103Asp
ENST00000676139.1:c.309G>C	ENSP00000502496.1:p.Glu103Asp
ENST00000676303.1:n.496G>C
ENST00000284476.7:c.309G>C	ENSP00000284476.6:p.Glu103Asp
ENST00000360254.3:n.629G>C
ENST00000482856.1:n.456G>C
NM_032890.3:c.309G>C	NP_116279.2:p.Glu103Asp
XM_005273335.1:c.309G>C	XP_005273392.1:p.Glu103Asp
XM_006711592.1:c.309G>C	XP_006711655.1:p.Glu103Asp
XM_011510072.1:c.309G>C	XP_011508374.1:p.Glu103Asp
XM_011510073.1:c.309G>C	XP_011508375.1:p.Glu103Asp
XM_011510074.1:c.309G>C	XP_011508376.1:p.Glu103Asp
XM_011510075.1:c.309G>C	XP_011508377.1:p.Glu103Asp
XM_011510076.1:c.309G>C	XP_011508378.1:p.Glu103Asp
XM_011510077.1:c.309G>C	XP_011508379.1:p.Glu103Asp
NM_001350630.1:c.-579G>C	NP_001337559.1:n.-579G>C
NM_032890.4:c.309G>C	NP_116279.2:p.Glu103Asp
XM_005273335.2:c.309G>C	XP_005273392.1:p.Glu103Asp
XM_006711592.2:c.309G>C	XP_006711655.1:p.Glu103Asp
XM_011510072.2:c.309G>C	XP_011508374.1:p.Glu103Asp
XM_011510073.2:c.309G>C	XP_011508375.1:p.Glu103Asp
XM_011510074.2:c.309G>C	XP_011508376.1:p.Glu103Asp
XM_011510075.2:c.309G>C	XP_011508377.1:p.Glu103Asp
XM_011510077.2:c.309G>C	XP_011508379.1:p.Glu103Asp
XM_017002611.1:c.309G>C	XP_016858100.1:p.Glu103Asp
NM_001350630.2:c.-579G>C	NP_001337559.1:n.-579G>C
NM_001369594.1:c.309G>C	NP_001356523.1:p.Glu103Asp
NM_001377228.1:c.309G>C	NP_001364157.1:p.Glu103Asp
NM_001377229.1:c.309G>C MANE Select	NP_001364158.1:p.Glu103Asp
NM_032890.5:c.309G>C	NP_116279.2:p.Glu103Asp