Canonical Allele Identifier: CA9569627

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49200386C>T , CM000681.2:g.49200386C>T	GRCh38
NC_000019.9:g.49703643C>T , CM000681.1:g.49703643C>T	GRCh37
NC_000019.8:g.54395455C>T	NCBI36
NG_027551.1:g.47628C>T
NG_027551.2:g.47628C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017636.4:c.2732C>T MANE Select	NP_060106.2:p.Thr911Met
ENST00000252826.10:c.2732C>T MANE Select	ENSP00000252826.4:p.Thr911Met
NM_001195227.1:c.2297C>T	NP_001182156.1:p.Thr766Met
NM_001195227.2:c.2297C>T	NP_001182156.1:p.Thr766Met
NM_001321281.1:c.2387C>T	NP_001308210.1:p.Thr796Met
NM_001321281.2:c.2387C>T	NP_001308210.1:p.Thr796Met
NM_001321282.1:c.1124C>T	NP_001308211.1:p.Thr375Met
NM_001321282.2:c.1124C>T	NP_001308211.1:p.Thr375Met
NM_001321283.1:c.2210C>T	NP_001308212.1:p.Thr737Met
NM_001321283.2:c.2210C>T	NP_001308212.1:p.Thr737Met
NM_001321285.1:c.1670C>T	NP_001308214.1:p.Thr557Met
NM_001321285.2:c.1670C>T	NP_001308214.1:p.Thr557Met
NM_017636.3:c.2732C>T	NP_060106.2:p.Thr911Met
ENST00000252826.9:c.2732C>T	ENSP00000252826.4:p.Thr911Met
ENST00000427978.6:c.2297C>T	ENSP00000407492.1:p.Thr766Met
ENST00000595071.5:n.1696C>T
ENST00000595519.5:c.*2142C>T	ENSP00000469893.1:n.*2142C>T
ENST00000596338.5:n.2829C>T
ENST00000598502.5:c.*1845C>T	ENSP00000470229.1:n.*1845C>T
ENST00000598697.5:c.*1687C>T	ENSP00000468989.1:n.*1687C>T
XM_005259017.1:c.1445C>T	XP_005259074.1:p.Thr482Met
XM_005259018.2:c.1124C>T	XP_005259075.1:p.Thr375Met
XM_011527046.1:c.2210C>T	XP_011525348.1:p.Thr737Met
XM_024451557.1:c.758C>T	XP_024307325.1:p.Thr253Met