Canonical Allele Identifier: CA14912335

Gene: TRPM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44434924G>A , CM000683.2:g.44434924G>A	GRCh38
NC_000021.8:g.45854807G>A , CM000683.1:g.45854807G>A	GRCh37
NC_000021.7:g.44679235G>A	NCBI36
NG_022913.1:g.86324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397928.6:c.3975-207G>A MANE Select	ENSP00000381023.1:n.3975-207G>A
ENST00000300481.13:c.3813-207G>A	ENSP00000300481.9:n.3813-207G>A
ENST00000300482.9:c.3975-207G>A	ENSP00000300482.5:n.3975-207G>A
ENST00000397928.5:c.3975-207G>A	ENSP00000381023.1:n.3975-207G>A
ENST00000397932.6:c.4125-207G>A	ENSP00000381026.2:n.4125-207G>A
ENST00000490982.1:n.310-207G>A
ENST00000498430.5:n.3427-207G>A
ENST00000621064.1:c.207-207G>A	ENSP00000477514.1:n.207-207G>A
NM_003307.3:c.3975-207G>A	NP_003298.1:n.3975-207G>A
NR_038257.1:n.4078-207G>A
XM_005261171.2:c.3975-207G>A	XP_005261228.1:n.3975-207G>A
XM_006724049.2:c.3873-207G>A	XP_006724112.1:n.3873-207G>A
XM_011529734.1:c.4125-207G>A	XP_011528036.1:n.4125-207G>A
XM_011529735.1:c.4125-207G>A	XP_011528037.1:n.4125-207G>A
XM_011529736.1:c.4065-207G>A	XP_011528038.1:n.4065-207G>A
XM_011529737.1:c.4023-207G>A	XP_011528039.1:n.4023-207G>A
XR_937565.1:n.4654-207G>A
NM_001320350.1:c.4125-207G>A	NP_001307279.1:n.4125-207G>A
NM_001320351.1:c.3873-207G>A	NP_001307280.1:n.3873-207G>A
NM_001320352.1:c.18-207G>A	NP_001307281.1:n.18-207G>A
XM_005261171.3:c.3975-207G>A	XP_005261228.1:n.3975-207G>A
XM_011529736.2:c.4065-207G>A	XP_011528038.1:n.4065-207G>A
XM_017028456.1:c.4065-207G>A	XP_016883945.1:n.4065-207G>A
XM_017028457.2:c.3963-207G>A	XP_016883946.1:n.3963-207G>A
XR_001754900.2:n.4708-207G>A
XR_001754901.2:n.4606-207G>A
XR_002958631.1:n.4839-207G>A
NM_001320350.2:c.4125-207G>A	NP_001307279.2:n.4125-207G>A
NM_001320351.2:c.3873-207G>A	NP_001307280.2:n.3873-207G>A
NM_001320352.3:c.18-207G>A	NP_001307281.1:n.18-207G>A
NM_003307.4:c.3975-207G>A MANE Select	NP_003298.2:n.3975-207G>A
NR_038257.2:n.4058-207G>A