Canonical Allele Identifier: CA354833356

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142804108A>G , CM000665.2:g.142804108A>G	GRCh38
NC_000003.11:g.142522950A>G , CM000665.1:g.142522950A>G	GRCh37
NC_000003.10:g.144005640A>G	NCBI36
NG_030369.1:g.84685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.2198A>G	ENSP00000513620.1:p.Asn733Ser
ENST00000476941.6:c.1889A>G MANE Select	ENSP00000419313.1:p.Asn630Ser
ENST00000273482.10:c.1787A>G	ENSP00000273482.6:p.Asn596Ser
ENST00000476941.5:c.1889A>G	ENSP00000419313.1:p.Asn630Ser
ENST00000612385.1:c.1787A>G	ENSP00000481537.1:p.Asn596Ser
NM_001251845.1:c.1889A>G	NP_001238774.1:p.Asn630Ser
NM_003304.4:c.1787A>G	NP_003295.1:p.Asn596Ser
XM_005247738.2:c.1595A>G	XP_005247795.1:p.Asn532Ser
XM_005247739.1:c.1493A>G	XP_005247796.1:p.Asn498Ser
XR_241506.2:n.2133A>G
XM_005247738.4:c.1595A>G	XP_005247795.1:p.Asn532Ser
XM_005247739.2:c.1493A>G	XP_005247796.1:p.Asn498Ser
XM_017007121.2:c.1706A>G	XP_016862610.1:p.Asn569Ser
XR_001740246.1:n.2724A>G
XR_241506.4:n.1656A>G
NM_001251845.2:c.1889A>G MANE Select	NP_001238774.1:p.Asn630Ser
NM_003304.5:c.1787A>G	NP_003295.1:p.Asn596Ser