Canonical Allele Identifier: CA2176471277

Gene: TRPM7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50586433G= , CM000677.2:g.50586433G=	GRCh38
NC_000015.9:g.50878630G= , CM000677.1:g.50878630G=	GRCh37
NC_000015.8:g.48665922G=	NCBI36
NG_021363.1:g.105383C=
NG_021363.2:g.105383C=

Transcript Alleles

HGVS	Amino-acid Change
NM_017672.6:c.4445C= MANE Select	NP_060142.3:p.Thr1482=
ENST00000646667.1:c.4445C= MANE Select	ENSP00000495860.1:p.Thr1482=
NM_001301212.1:c.4445C=	NP_001288141.1:p.Thr1482=
NM_001301212.2:c.4445C=	NP_001288141.1:p.Thr1482=
NM_017672.5:c.4445C=	NP_060142.3:p.Thr1482=
NR_149152.1:n.4677C=
NR_149152.2:n.4659C=
NR_149153.1:n.4600C=
NR_149153.2:n.4582C=
NR_149154.1:n.4527C=
NR_149154.2:n.4509C=
ENST00000313478.11:c.4445C=	ENSP00000320239.7:p.Thr1482=
ENST00000560849.2:n.150C=
ENST00000560955.5:c.4445C=	ENSP00000453277.1:p.Thr1482=
ENST00000645282.1:n.249C=
XM_005254486.2:c.4505C=	XP_005254543.1:p.Thr1502=
XM_005254486.4:c.4505C=	XP_005254543.1:p.Thr1502=
XM_005254487.2:c.4505C=	XP_005254544.1:p.Thr1502=
XM_017022350.1:c.4532C=	XP_016877839.1:p.Thr1511=
XM_017022351.1:c.4532C=	XP_016877840.1:p.Thr1511=
XM_017022352.1:c.4472C=	XP_016877841.1:p.Thr1491=
XM_017022353.2:c.4472C=	XP_016877842.1:p.Thr1491=
XM_017022354.1:c.4328C=	XP_016877843.1:p.Thr1443=
XM_017022355.1:c.4328C=	XP_016877844.1:p.Thr1443=
XR_001751325.1:n.4547C=
XR_001751326.2:n.4547C=
XR_001751327.1:n.4547C=
XR_001751328.2:n.4547C=
XR_002957654.1:n.4437C=
XR_931853.1:n.4787C=