Canonical Allele Identifier: CA10054974

Gene: TRPM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44401911C>T , CM000683.2:g.44401911C>T	GRCh38
NC_000021.8:g.45821794C>T , CM000683.1:g.45821794C>T	GRCh37
NC_000021.7:g.44646222C>T	NCBI36
NG_022913.1:g.53311C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397928.6:c.2538+14C>T MANE Select	ENSP00000381023.1:n.2538+14C>T
ENST00000300481.13:c.2478+14C>T	ENSP00000300481.9:n.2478+14C>T
ENST00000300482.9:c.2538+14C>T	ENSP00000300482.5:n.2538+14C>T
ENST00000397928.5:c.2538+14C>T	ENSP00000381023.1:n.2538+14C>T
ENST00000397932.6:c.2538+14C>T	ENSP00000381026.2:n.2538+14C>T
ENST00000498430.5:n.1990+14C>T
NM_003307.3:c.2538+14C>T	NP_003298.1:n.2538+14C>T
NR_038257.1:n.2638+14C>T
XM_005261171.2:c.2538+14C>T	XP_005261228.1:n.2538+14C>T
XM_006724049.2:c.2538+14C>T	XP_006724112.1:n.2538+14C>T
XM_011529734.1:c.2538+14C>T	XP_011528036.1:n.2538+14C>T
XM_011529735.1:c.2538+14C>T	XP_011528037.1:n.2538+14C>T
XM_011529736.1:c.2538+14C>T	XP_011528038.1:n.2538+14C>T
XM_011529737.1:c.2538+14C>T	XP_011528039.1:n.2538+14C>T
XR_937565.1:n.3033+14C>T
XR_937566.1:n.3032+14C>T
NM_001320350.1:c.2538+14C>T	NP_001307279.1:n.2538+14C>T
NM_001320351.1:c.2538+14C>T	NP_001307280.1:n.2538+14C>T
XM_005261171.3:c.2538+14C>T	XP_005261228.1:n.2538+14C>T
XM_011529736.2:c.2538+14C>T	XP_011528038.1:n.2538+14C>T
XM_017028456.1:c.2538+14C>T	XP_016883945.1:n.2538+14C>T
XM_017028457.2:c.2538+14C>T	XP_016883946.1:n.2538+14C>T
XR_001754900.2:n.3045+14C>T
XR_001754901.2:n.3045+14C>T
XR_001754902.2:n.3043+14C>T
XR_002958631.1:n.3046+14C>T
NM_001320350.2:c.2538+14C>T	NP_001307279.2:n.2538+14C>T
NM_001320351.2:c.2538+14C>T	NP_001307280.2:n.2538+14C>T
NM_003307.4:c.2538+14C>T MANE Select	NP_003298.2:n.2538+14C>T
NR_038257.2:n.2618+14C>T