Canonical Allele Identifier: CA2838001804

Gene: TRPC7 TRPC7-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.136240141C>G , CM000667.2:g.136240141C>G	GRCh38
NC_000005.9:g.135575829C>G , CM000667.1:g.135575829C>G	GRCh37
NC_000005.8:g.135603728C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352189.8:c.1496+7330G>C (TRPC7)	ENSP00000330322.5:n.1496+7330G>C
ENST00000378459.7:c.1661+7330G>C (TRPC7)	ENSP00000367720.3:n.1661+7330G>C
ENST00000502753.4:c.1679+7330G>C (TRPC7)	ENSP00000424854.3:n.1679+7330G>C
ENST00000503275.6:c.*717+7330G>C (TRPC7)	ENSP00000421571.2:n.*717+7330G>C
ENST00000513104.6:c.1844+7330G>C (TRPC7) MANE Select	ENSP00000426070.2:n.1844+7330G>C
ENST00000352189.7:c.1496+7330G>C (TRPC7)	ENSP00000330322.5:n.1496+7330G>C
ENST00000378459.6:c.1661+7330G>C (TRPC7)	ENSP00000367720.3:n.1661+7330G>C
ENST00000502753.3:c.1679+7330G>C (TRPC7)	ENSP00000424854.3:n.1679+7330G>C
ENST00000503275.5:c.1860+7330G>C (TRPC7)	ENSP00000421571.2:n.1860+7330G>C
ENST00000513104.5:c.1844+7330G>C (TRPC7)	ENSP00000426070.1:n.1844+7330G>C
ENST00000514963.5:c.1279+7330G>C (TRPC7)	ENSP00000426870.2:n.1279+7330G>C
NM_001167576.1:c.1496+7330G>C (TRPC7)	NP_001161048.1:n.1496+7330G>C
NM_001167577.1:c.1661+7330G>C (TRPC7)	NP_001161049.1:n.1661+7330G>C
NM_020389.2:c.1844+7330G>C (TRPC7)	NP_065122.1:n.1844+7330G>C
XM_011543516.1:c.1817+7330G>C (TRPC7)	XP_011541818.1:n.1817+7330G>C
XM_011543517.1:c.1652+7330G>C (TRPC7)	XP_011541819.1:n.1652+7330G>C
XM_011543518.1:c.1649+7330G>C (TRPC7)	XP_011541820.1:n.1649+7330G>C
NR_133682.1:n.59+13428C>G (TRPC7-AS2)
NM_001167576.2:c.1496+7330G>C (TRPC7)	NP_001161048.1:n.1496+7330G>C
NM_001167577.2:c.1661+7330G>C (TRPC7)	NP_001161049.1:n.1661+7330G>C
NM_001376901.1:c.1679+7330G>C (TRPC7)	NP_001363830.1:n.1679+7330G>C
NM_020389.3:c.1844+7330G>C (TRPC7) MANE Select	NP_065122.1:n.1844+7330G>C