Canonical Allele Identifier: CA174738

Gene: CRTC3 CRTC3-AS1

Linked Data

• ClinVar Variation Id: 161762
• ClinVar RCV Id: RCV000149298
• dbSNP Id: rs193921108
• COSMIC: COSM5521448
• MyVariant Identifiers: chr15:g.91181798C>A (hg19) ; chr15:g.90638566C>A (hg38)
• PubMed: PMID:23265383

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90638566C>A , CM000677.2:g.90638566C>A	GRCh38
NC_000015.9:g.91181798C>A , CM000677.1:g.91181798C>A	GRCh37
NC_000015.8:g.88982802C>A	NCBI36
NG_047180.1:g.113681C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686240.1:c.*800C>A (CRTC3)	ENSP00000508866.1:n.*800C>A
ENST00000691029.1:c.1387C>A (CRTC3)	ENSP00000510507.1:p.Arg463Ser
ENST00000692149.1:c.1200C>A (CRTC3)	ENSP00000510448.1:n.1200C>A
ENST00000268184.11:c.1387C>A (CRTC3) MANE Select	ENSP00000268184.6:p.Arg463Ser
ENST00000268184.10:c.1387C>A (CRTC3)	ENSP00000268184.6:p.Arg463Ser
ENST00000420329.6:c.1387C>A (CRTC3)	ENSP00000416573.2:p.Arg463Ser
NM_001042574.2:c.1387C>A (CRTC3)	NP_001036039.1:p.Arg463Ser
NM_022769.4:c.1387C>A (CRTC3)	NP_073606.3:p.Arg463Ser
NR_120372.1:n.509+2476G>T (CRTC3-AS1)
XM_005254968.1:c.1384C>A (CRTC3)	XP_005255025.1:p.Arg462Ser
XM_011521906.1:c.1288C>A (CRTC3)	XP_011520208.1:p.Arg430Ser
XM_005254968.2:c.1384C>A (CRTC3)	XP_005255025.1:p.Arg462Ser
XM_011521906.2:c.1288C>A (CRTC3)	XP_011520208.1:p.Arg430Ser
XM_024450018.1:c.814C>A (CRTC3)	XP_024305786.1:p.Arg272Ser
XM_024450019.1:c.814C>A (CRTC3)	XP_024305787.1:p.Arg272Ser
NM_022769.5:c.1387C>A (CRTC3) MANE Select	NP_073606.3:p.Arg463Ser
NM_001042574.3:c.1387C>A (CRTC3)	NP_001036039.1:p.Arg463Ser