Canonical Allele Identifier: CA321772326

Gene: TRPM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44391460T>C , CM000683.2:g.44391460T>C	GRCh38
NC_000021.8:g.45811343T>C , CM000683.1:g.45811343T>C	GRCh37
NC_000021.7:g.44635771T>C	NCBI36
NG_022913.1:g.42860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397928.6:c.1629T>C MANE Select	ENSP00000381023.1:p.Asp543=
ENST00000300481.13:c.1611+18T>C	ENSP00000300481.9:n.1611+18T>C
ENST00000300482.9:c.1629T>C	ENSP00000300482.5:p.Asp543=
ENST00000397928.5:c.1629T>C	ENSP00000381023.1:p.Asp543=
ENST00000397932.6:c.1629T>C	ENSP00000381026.2:p.Asp543=
ENST00000498430.5:n.1081T>C
NM_003307.3:c.1629T>C	NP_003298.1:p.Asp543=
NR_038257.1:n.1729T>C
XM_005261171.2:c.1629T>C	XP_005261228.1:p.Asp543=
XM_006724049.2:c.1629T>C	XP_006724112.1:p.Asp543=
XM_011529734.1:c.1629T>C	XP_011528036.1:p.Asp543=
XM_011529735.1:c.1629T>C	XP_011528037.1:p.Asp543=
XM_011529736.1:c.1629T>C	XP_011528038.1:p.Asp543=
XM_011529737.1:c.1629T>C	XP_011528039.1:p.Asp543=
XR_937565.1:n.2124T>C
XR_937566.1:n.2123T>C
NM_001320350.1:c.1629T>C	NP_001307279.1:p.Asp543=
NM_001320351.1:c.1629T>C	NP_001307280.1:p.Asp543=
XM_005261171.3:c.1629T>C	XP_005261228.1:p.Asp543=
XM_011529736.2:c.1629T>C	XP_011528038.1:p.Asp543=
XM_017028456.1:c.1629T>C	XP_016883945.1:p.Asp543=
XM_017028457.2:c.1629T>C	XP_016883946.1:p.Asp543=
XR_001754900.2:n.2136T>C
XR_001754901.2:n.2136T>C
XR_001754902.2:n.2134T>C
XR_002958631.1:n.2137T>C
NM_001320350.2:c.1629T>C	NP_001307279.2:p.Asp543=
NM_001320351.2:c.1629T>C	NP_001307280.2:p.Asp543=
NM_003307.4:c.1629T>C MANE Select	NP_003298.2:p.Asp543=
NR_038257.2:n.1709T>C