Canonical Allele Identifier: CA994239960
Gene: CRTC1 HGNC NCBI

Linked Data

dbSNP Id: rs2052858021

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18692168_18692169insTT , CM000681.2:g.18692168_18692169insTT GRCh38
NC_000019.9:g.18802978_18802979insTT , CM000681.1:g.18802978_18802979insTT GRCh37
NC_000019.8:g.18663978_18663979insTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321949.13:c.126+8340_126+8341insTT MANE Select ENSP00000323332.7:n.126+8340_126+8341insTT
ENST00000321949.12:c.126+8340_126+8341insTT ENSP00000323332.7:n.126+8340_126+8341insTT
ENST00000338797.10:c.126+8340_126+8341insTT ENSP00000345001.5:n.126+8340_126+8341insTT
NM_001098482.1:c.126+8340_126+8341insTT NP_001091952.1:n.126+8340_126+8341insTT
NM_015321.2:c.126+8340_126+8341insTT NP_056136.2:n.126+8340_126+8341insTT
XM_005259833.2:c.126+8340_126+8341insTT XP_005259890.1:n.126+8340_126+8341insTT
XM_005259834.1:c.126+8340_126+8341insTT XP_005259891.1:n.126+8340_126+8341insTT
XM_005259835.2:c.126+8340_126+8341insTT XP_005259892.1:n.126+8340_126+8341insTT
XM_005259836.2:c.126+8340_126+8341insTT XP_005259893.1:n.126+8340_126+8341insTT
XM_006722710.2:c.126+8340_126+8341insTT XP_006722773.1:n.126+8340_126+8341insTT
XM_011527842.1:c.126+8340_126+8341insTT XP_011526144.1:n.126+8340_126+8341insTT
XM_005259833.3:c.126+8340_126+8341insTT XP_005259890.1:n.126+8340_126+8341insTT
XM_005259835.3:c.126+8340_126+8341insTT XP_005259892.1:n.126+8340_126+8341insTT
XM_005259836.3:c.126+8340_126+8341insTT XP_005259893.1:n.126+8340_126+8341insTT
XM_006722710.3:c.126+8340_126+8341insTT XP_006722773.1:n.126+8340_126+8341insTT
XM_011527842.3:c.126+8340_126+8341insTT XP_011526144.1:n.126+8340_126+8341insTT
XM_017026536.1:c.126+8340_126+8341insTT XP_016882025.1:n.126+8340_126+8341insTT
XM_017026537.1:c.126+8340_126+8341insTT XP_016882026.1:n.126+8340_126+8341insTT
XM_017026538.2:c.126+8340_126+8341insTT XP_016882027.1:n.126+8340_126+8341insTT
XM_024451434.1:c.126+8340_126+8341insTT XP_024307202.1:n.126+8340_126+8341insTT
NM_015321.3:c.126+8340_126+8341insTT MANE Select NP_056136.2:n.126+8340_126+8341insTT
NM_001098482.2:c.126+8340_126+8341insTT NP_001091952.1:n.126+8340_126+8341insTT