Canonical Allele Identifier: CA2326478817

Gene: CRTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18692362T>C , CM000681.2:g.18692362T>C	GRCh38
NC_000019.9:g.18803172T>C , CM000681.1:g.18803172T>C	GRCh37
NC_000019.8:g.18664172T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015321.3:c.126+8534T>C MANE Select	NP_056136.2:n.126+8534T>C
ENST00000321949.13:c.126+8534T>C MANE Select	ENSP00000323332.7:n.126+8534T>C
NM_001098482.1:c.126+8534T>C	NP_001091952.1:n.126+8534T>C
NM_001098482.2:c.126+8534T>C	NP_001091952.1:n.126+8534T>C
NM_015321.2:c.126+8534T>C	NP_056136.2:n.126+8534T>C
ENST00000321949.12:c.126+8534T>C	ENSP00000323332.7:n.126+8534T>C
ENST00000338797.10:c.126+8534T>C	ENSP00000345001.5:n.126+8534T>C
XM_005259833.2:c.126+8534T>C	XP_005259890.1:n.126+8534T>C
XM_005259833.3:c.126+8534T>C	XP_005259890.1:n.126+8534T>C
XM_005259834.1:c.126+8534T>C	XP_005259891.1:n.126+8534T>C
XM_005259835.2:c.126+8534T>C	XP_005259892.1:n.126+8534T>C
XM_005259835.3:c.126+8534T>C	XP_005259892.1:n.126+8534T>C
XM_005259836.2:c.126+8534T>C	XP_005259893.1:n.126+8534T>C
XM_005259836.3:c.126+8534T>C	XP_005259893.1:n.126+8534T>C
XM_006722710.2:c.126+8534T>C	XP_006722773.1:n.126+8534T>C
XM_006722710.3:c.126+8534T>C	XP_006722773.1:n.126+8534T>C
XM_011527842.1:c.126+8534T>C	XP_011526144.1:n.126+8534T>C
XM_011527842.3:c.126+8534T>C	XP_011526144.1:n.126+8534T>C
XM_017026536.1:c.126+8534T>C	XP_016882025.1:n.126+8534T>C
XM_017026537.1:c.126+8534T>C	XP_016882026.1:n.126+8534T>C
XM_017026538.2:c.126+8534T>C	XP_016882027.1:n.126+8534T>C
XM_024451434.1:c.126+8534T>C	XP_024307202.1:n.126+8534T>C