Canonical Allele Identifier: CA9569050

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49171782_49171785dup , CM000681.2:g.49171782_49171785dup	GRCh38
NC_000019.9:g.49675039_49675042dup , CM000681.1:g.49675039_49675042dup	GRCh37
NC_000019.8:g.54366851_54366854dup	NCBI36
NG_027551.1:g.19024_19027dup
NG_027551.2:g.19024_19027dup

Transcript Alleles

HGVS	Amino-acid Change
NM_017636.4:c.1050+13_1050+16dup MANE Select	NP_060106.2:n.1050+13_1050+16dup
ENST00000252826.10:c.1050+13_1050+16dup MANE Select	ENSP00000252826.4:n.1050+13_1050+16dup
NM_001195227.1:c.1050+13_1050+16dup	NP_001182156.1:n.1050+13_1050+16dup
NM_001195227.2:c.1050+13_1050+16dup	NP_001182156.1:n.1050+13_1050+16dup
NM_001321281.1:c.705+13_705+16dup	NP_001308210.1:n.705+13_705+16dup
NM_001321281.2:c.705+13_705+16dup	NP_001308210.1:n.705+13_705+16dup
NM_001321282.1:c.-504+13_-504+16dup	NP_001308211.1:n.-504+13_-504+16dup
NM_001321282.2:c.-504+13_-504+16dup	NP_001308211.1:n.-504+13_-504+16dup
NM_001321283.1:c.528+13_528+16dup	NP_001308212.1:n.528+13_528+16dup
NM_001321283.2:c.528+13_528+16dup	NP_001308212.1:n.528+13_528+16dup
NM_001321285.1:c.201+13_201+16dup	NP_001308214.1:n.201+13_201+16dup
NM_001321285.2:c.201+13_201+16dup	NP_001308214.1:n.201+13_201+16dup
NM_017636.3:c.1050+13_1050+16dup	NP_060106.2:n.1050+13_1050+16dup
ENST00000252826.9:c.1050+13_1050+16dup	ENSP00000252826.4:n.1050+13_1050+16dup
ENST00000427978.6:c.1050+13_1050+16dup	ENSP00000407492.1:n.1050+13_1050+16dup
ENST00000595519.5:c.*460+13_*460+16dup	ENSP00000469893.1:n.*460+13_*460+16dup
ENST00000596338.5:n.1085+13_1085+16dup
ENST00000598502.5:c.*218+13_*218+16dup	ENSP00000470229.1:n.*218+13_*218+16dup
ENST00000598697.5:c.*218+13_*218+16dup	ENSP00000468989.1:n.*218+13_*218+16dup
ENST00000601347.1:n.364+13_364+16dup
XM_005259017.1:c.-125+13_-125+16dup	XP_005259074.1:n.-125+13_-125+16dup
XM_011527046.1:c.528+13_528+16dup	XP_011525348.1:n.528+13_528+16dup
XM_024451557.1:c.-1045+13_-1045+16dup	XP_024307325.1:n.-1045+13_-1045+16dup