Canonical Allele Identifier: CA2326478805

Gene: CRTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18692342_18692343delinsCA , CM000681.2:g.18692342_18692343delinsCA	GRCh38
NC_000019.9:g.18803152_18803153delinsCA , CM000681.1:g.18803152_18803153delinsCA	GRCh37
NC_000019.8:g.18664152_18664153delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321949.13:c.126+8514_126+8515delinsCA MANE Select	ENSP00000323332.7:n.126+8514_126+8515delinsCA
ENST00000321949.12:c.126+8514_126+8515delinsCA	ENSP00000323332.7:n.126+8514_126+8515delinsCA
ENST00000338797.10:c.126+8514_126+8515delinsCA	ENSP00000345001.5:n.126+8514_126+8515delinsCA
NM_001098482.1:c.126+8514_126+8515delinsCA	NP_001091952.1:n.126+8514_126+8515delinsCA
NM_015321.2:c.126+8514_126+8515delinsCA	NP_056136.2:n.126+8514_126+8515delinsCA
XM_005259833.2:c.126+8514_126+8515delinsCA	XP_005259890.1:n.126+8514_126+8515delinsCA
XM_005259834.1:c.126+8514_126+8515delinsCA	XP_005259891.1:n.126+8514_126+8515delinsCA
XM_005259835.2:c.126+8514_126+8515delinsCA	XP_005259892.1:n.126+8514_126+8515delinsCA
XM_005259836.2:c.126+8514_126+8515delinsCA	XP_005259893.1:n.126+8514_126+8515delinsCA
XM_006722710.2:c.126+8514_126+8515delinsCA	XP_006722773.1:n.126+8514_126+8515delinsCA
XM_011527842.1:c.126+8514_126+8515delinsCA	XP_011526144.1:n.126+8514_126+8515delinsCA
XM_005259833.3:c.126+8514_126+8515delinsCA	XP_005259890.1:n.126+8514_126+8515delinsCA
XM_005259835.3:c.126+8514_126+8515delinsCA	XP_005259892.1:n.126+8514_126+8515delinsCA
XM_005259836.3:c.126+8514_126+8515delinsCA	XP_005259893.1:n.126+8514_126+8515delinsCA
XM_006722710.3:c.126+8514_126+8515delinsCA	XP_006722773.1:n.126+8514_126+8515delinsCA
XM_011527842.3:c.126+8514_126+8515delinsCA	XP_011526144.1:n.126+8514_126+8515delinsCA
XM_017026536.1:c.126+8514_126+8515delinsCA	XP_016882025.1:n.126+8514_126+8515delinsCA
XM_017026537.1:c.126+8514_126+8515delinsCA	XP_016882026.1:n.126+8514_126+8515delinsCA
XM_017026538.2:c.126+8514_126+8515delinsCA	XP_016882027.1:n.126+8514_126+8515delinsCA
XM_024451434.1:c.126+8514_126+8515delinsCA	XP_024307202.1:n.126+8514_126+8515delinsCA
NM_015321.3:c.126+8514_126+8515delinsCA MANE Select	NP_056136.2:n.126+8514_126+8515delinsCA
NM_001098482.2:c.126+8514_126+8515delinsCA	NP_001091952.1:n.126+8514_126+8515delinsCA