Canonical Allele Identifier: CA2326515076
Gene: CRTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18765509C= , CM000681.2:g.18765509C= GRCh38
NC_000019.9:g.18876319C= , CM000681.1:g.18876319C= GRCh37
NC_000019.8:g.18737319C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321949.13:c.992C= MANE Select ENSP00000323332.7:p.Pro331=
ENST00000321949.12:c.992C= ENSP00000323332.7:p.Pro331=
ENST00000338797.10:c.1040C= ENSP00000345001.5:p.Pro347=
ENST00000594658.5:c.869C= ENSP00000468893.1:p.Pro290=
ENST00000601916.1:c.767C= ENSP00000469285.1:p.Pro256=
NM_001098482.1:c.1040C= NP_001091952.1:p.Pro347=
NM_015321.2:c.992C= NP_056136.2:p.Pro331=
XM_005259833.2:c.1040C= XP_005259890.1:p.Pro347=
XM_005259834.1:c.992C= XP_005259891.1:p.Pro331=
XM_005259835.2:c.1040C= XP_005259892.1:p.Pro347=
XM_005259836.2:c.1040C= XP_005259893.1:p.Pro347=
XM_006722710.2:c.1040C= XP_006722773.1:p.Pro347=
XM_011527842.1:c.1040C= XP_011526144.1:p.Pro347=
XM_005259833.3:c.1040C= XP_005259890.1:p.Pro347=
XM_005259835.3:c.1040C= XP_005259892.1:p.Pro347=
XM_005259836.3:c.1040C= XP_005259893.1:p.Pro347=
XM_006722710.3:c.1040C= XP_006722773.1:p.Pro347=
XM_011527842.3:c.1040C= XP_011526144.1:p.Pro347=
XM_017026536.1:c.1040C= XP_016882025.1:p.Pro347=
XM_017026537.1:c.1040C= XP_016882026.1:p.Pro347=
XM_024451434.1:c.992C= XP_024307202.1:p.Pro331=
NM_015321.3:c.992C= MANE Select NP_056136.2:p.Pro331=
NM_001098482.2:c.1040C= NP_001091952.1:p.Pro347=