Canonical Allele Identifier: CA2195189457

Gene: CRTC3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90571144A>T , CM000677.2:g.90571144A>T	GRCh38
NC_000015.9:g.91114376A>T , CM000677.1:g.91114376A>T	GRCh37
NC_000015.8:g.88915380A>T	NCBI36
NG_047180.1:g.46259A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686240.1:c.232-22492A>T	ENSP00000508866.1:n.232-22492A>T
ENST00000687075.1:c.57-22492A>T
ENST00000691029.1:c.232-22492A>T	ENSP00000510507.1:n.232-22492A>T
ENST00000692149.1:c.232-22492A>T	ENSP00000510448.1:n.232-22492A>T
ENST00000268184.11:c.232-22492A>T MANE Select	ENSP00000268184.6:n.232-22492A>T
ENST00000268184.10:c.232-22492A>T	ENSP00000268184.6:n.232-22492A>T
ENST00000420329.6:c.232-22492A>T	ENSP00000416573.2:n.232-22492A>T
ENST00000558619.5:n.316-22492A>T
ENST00000560098.5:c.232-27306A>T	ENSP00000452640.1:n.232-27306A>T
ENST00000560927.1:n.522-22492A>T
ENST00000561218.5:n.241-29164A>T
NM_001042574.2:c.232-22492A>T	NP_001036039.1:n.232-22492A>T
NM_022769.4:c.232-22492A>T	NP_073606.3:n.232-22492A>T
XM_005254968.1:c.232-22492A>T	XP_005255025.1:n.232-22492A>T
XM_011521906.1:c.133-22492A>T	XP_011520208.1:n.133-22492A>T
XM_005254968.2:c.232-22492A>T	XP_005255025.1:n.232-22492A>T
XM_011521906.2:c.133-22492A>T	XP_011520208.1:n.133-22492A>T
NM_022769.5:c.232-22492A>T MANE Select	NP_073606.3:n.232-22492A>T
NM_001042574.3:c.232-22492A>T	NP_001036039.1:n.232-22492A>T