Canonical Allele Identifier: CA2195216828

Gene: CRTC3 CRTC3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90629669C= , CM000677.2:g.90629669C=	GRCh38
NC_000015.9:g.91172901C= , CM000677.1:g.91172901C=	GRCh37
NC_000015.8:g.88973905C=	NCBI36
NG_047180.1:g.104784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686240.1:c.*679+137C= (CRTC3)	ENSP00000508866.1:n.*679+137C=
ENST00000691029.1:c.1266+137C= (CRTC3)	ENSP00000510507.1:n.1266+137C=
ENST00000692149.1:c.1079+137C= (CRTC3)	ENSP00000510448.1:n.1079+137C=
ENST00000268184.11:c.1266+137C= (CRTC3) MANE Select	ENSP00000268184.6:n.1266+137C=
ENST00000268184.10:c.1266+137C= (CRTC3)	ENSP00000268184.6:n.1266+137C=
ENST00000420329.6:c.1266+137C= (CRTC3)	ENSP00000416573.2:n.1266+137C=
NM_001042574.2:c.1266+137C= (CRTC3)	NP_001036039.1:n.1266+137C=
NM_022769.4:c.1266+137C= (CRTC3)	NP_073606.3:n.1266+137C=
NR_120372.1:n.510-9516G= (CRTC3-AS1)
XM_005254968.1:c.1263+137C= (CRTC3)	XP_005255025.1:n.1263+137C=
XM_011521906.1:c.1167+137C= (CRTC3)	XP_011520208.1:n.1167+137C=
XM_005254968.2:c.1263+137C= (CRTC3)	XP_005255025.1:n.1263+137C=
XM_011521906.2:c.1167+137C= (CRTC3)	XP_011520208.1:n.1167+137C=
XM_024450018.1:c.693+137C= (CRTC3)	XP_024305786.1:n.693+137C=
XM_024450019.1:c.693+137C= (CRTC3)	XP_024305787.1:n.693+137C=
NM_022769.5:c.1266+137C= (CRTC3) MANE Select	NP_073606.3:n.1266+137C=
NM_001042574.3:c.1266+137C= (CRTC3)	NP_001036039.1:n.1266+137C=