Canonical Allele Identifier: CA2326523329

Gene: CRTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18781850T= , CM000681.2:g.18781850T=	GRCh38
NC_000019.9:g.18892660T= , CM000681.1:g.18892660T=	GRCh37
NC_000019.8:g.18753660T=	NCBI36
NG_007070.1:g.14455A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321949.13:c.*4468T= MANE Select	ENSP00000323332.7:n.*4468T=
ENST00000338797.10:c.*4468T=	ENSP00000345001.5:n.*4468T=
NM_001098482.1:c.*4468T=	NP_001091952.1:n.*4468T=
NM_015321.2:c.*4468T=	NP_056136.2:n.*4468T=
XM_005259833.2:c.*4468T=	XP_005259890.1:n.*4468T=
XM_005259834.1:c.*4468T=	XP_005259891.1:n.*4468T=
XM_005259835.2:c.*4468T=	XP_005259892.1:n.*4468T=
XM_005259836.2:c.*4468T=	XP_005259893.1:n.*4468T=
XM_006722710.2:c.*4468T=	XP_006722773.1:n.*4468T=
XM_011527842.1:c.*4468T=	XP_011526144.1:n.*4468T=
XM_005259833.3:c.*4468T=	XP_005259890.1:n.*4468T=
XM_005259835.3:c.*4468T=	XP_005259892.1:n.*4468T=
XM_005259836.3:c.*4468T=	XP_005259893.1:n.*4468T=
XM_006722710.3:c.*4468T=	XP_006722773.1:n.*4468T=
XM_011527842.3:c.*4468T=	XP_011526144.1:n.*4468T=
XM_024451434.1:c.*4468T=	XP_024307202.1:n.*4468T=
NM_015321.3:c.*4468T= MANE Select	NP_056136.2:n.*4468T=
NM_001098482.2:c.*4468T=	NP_001091952.1:n.*4468T=