Canonical Allele Identifier: CA2651502
Community Standard Title: NM_001251845.2(TRPC1):c.106G>A (p.Asp36Asn)
Gene: TRPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142724665G>A , CM000665.2:g.142724665G>A GRCh38
NC_000003.11:g.142443507G>A , CM000665.1:g.142443507G>A GRCh37
NC_000003.10:g.143926197G>A NCBI36
NG_030369.1:g.5242G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001251845.2:c.106G>A MANE Select NP_001238774.1:p.Asp36Asn
ENST00000476941.6:c.106G>A MANE Select ENSP00000419313.1:p.Asp36Asn
NM_001251845.1:c.106G>A NP_001238774.1:p.Asp36Asn
NM_003304.4:c.106G>A NP_003295.1:p.Asp36Asn
NM_003304.5:c.106G>A NP_003295.1:p.Asp36Asn
ENST00000273482.10:c.106G>A ENSP00000273482.6:p.Asp36Asn
ENST00000460401.1:c.101G>A
ENST00000476941.5:c.106G>A ENSP00000419313.1:p.Asp36Asn
ENST00000612385.1:c.106G>A ENSP00000481537.1:p.Asp36Asn
ENST00000698238.1:c.415G>A ENSP00000513620.1:p.Asp139Asn
XM_005247738.2:c.-34G>A XP_005247795.1:n.-34G>A
XM_005247738.4:c.-34G>A XP_005247795.1:n.-34G>A
XM_005247739.1:c.-34G>A XP_005247796.1:n.-34G>A
XM_005247739.2:c.-34G>A XP_005247796.1:n.-34G>A
XR_241506.2:n.634G>A
XR_241506.4:n.157G>A
XR_924164.1:n.634G>A
XR_924165.1:n.634G>A
XR_924166.1:n.634G>A