Canonical Allele Identifier: CA392395278

Gene: TRPM7

Linked Data

• dbSNP Id: rs8042919
• gnomAD v2: 15-50878630-G-T
• gnomAD v4: 15-50586433-G-T
• MyVariant Identifiers: chr15:g.50878630G>T (hg19) ; chr15:g.50586433G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000645282.1:n.249C>A
ENST00000646667.1:c.4445C>A MANE Select	ENSP00000495860.1:p.Thr1482Asn
ENST00000313478.11:c.4445C>A	ENSP00000320239.7:p.Thr1482Asn
ENST00000560849.2:n.150C>A
ENST00000560955.5:c.4445C>A	ENSP00000453277.1:p.Thr1482Asn
NM_001301212.1:c.4445C>A	NP_001288141.1:p.Thr1482Asn
NM_017672.5:c.4445C>A	NP_060142.3:p.Thr1482Asn
XM_005254486.2:c.4505C>A	XP_005254543.1:p.Thr1502Asn
XM_005254487.2:c.4505C>A	XP_005254544.1:p.Thr1502Asn
XR_931853.1:n.4787C>A
NR_149152.1:n.4677C>A
NR_149153.1:n.4600C>A
NR_149154.1:n.4527C>A
XM_005254486.4:c.4505C>A	XP_005254543.1:p.Thr1502Asn
XM_017022350.1:c.4532C>A	XP_016877839.1:p.Thr1511Asn
XM_017022351.1:c.4532C>A	XP_016877840.1:p.Thr1511Asn
XM_017022352.1:c.4472C>A	XP_016877841.1:p.Thr1491Asn
XM_017022353.2:c.4472C>A	XP_016877842.1:p.Thr1491Asn
XM_017022354.1:c.4328C>A	XP_016877843.1:p.Thr1443Asn
XM_017022355.1:c.4328C>A	XP_016877844.1:p.Thr1443Asn
XR_001751325.1:n.4547C>A
XR_001751326.2:n.4547C>A
XR_001751327.1:n.4547C>A
XR_001751328.2:n.4547C>A
XR_002957654.1:n.4437C>A
NM_017672.6:c.4445C>A MANE Select	NP_060142.3:p.Thr1482Asn
NM_001301212.2:c.4445C>A	NP_001288141.1:p.Thr1482Asn
NR_149152.2:n.4659C>A
NR_149153.2:n.4582C>A
NR_149154.2:n.4509C>A