Canonical Allele Identifier: CA2326515051

Gene: CRTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18765448G= , CM000681.2:g.18765448G=	GRCh38
NC_000019.9:g.18876258G= , CM000681.1:g.18876258G=	GRCh37
NC_000019.8:g.18737258G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015321.3:c.931G= MANE Select	NP_056136.2:p.Val311=
ENST00000321949.13:c.931G= MANE Select	ENSP00000323332.7:p.Val311=
NM_001098482.1:c.979G=	NP_001091952.1:p.Val327=
NM_001098482.2:c.979G=	NP_001091952.1:p.Val327=
NM_015321.2:c.931G=	NP_056136.2:p.Val311=
ENST00000321949.12:c.931G=	ENSP00000323332.7:p.Val311=
ENST00000338797.10:c.979G=	ENSP00000345001.5:p.Val327=
ENST00000594658.5:c.808G=	ENSP00000468893.1:p.Val270=
ENST00000601916.1:c.706G=	ENSP00000469285.1:p.Val236=
XM_005259833.2:c.979G=	XP_005259890.1:p.Val327=
XM_005259833.3:c.979G=	XP_005259890.1:p.Val327=
XM_005259834.1:c.931G=	XP_005259891.1:p.Val311=
XM_005259835.2:c.979G=	XP_005259892.1:p.Val327=
XM_005259835.3:c.979G=	XP_005259892.1:p.Val327=
XM_005259836.2:c.979G=	XP_005259893.1:p.Val327=
XM_005259836.3:c.979G=	XP_005259893.1:p.Val327=
XM_006722710.2:c.979G=	XP_006722773.1:p.Val327=
XM_006722710.3:c.979G=	XP_006722773.1:p.Val327=
XM_011527842.1:c.979G=	XP_011526144.1:p.Val327=
XM_011527842.3:c.979G=	XP_011526144.1:p.Val327=
XM_017026536.1:c.979G=	XP_016882025.1:p.Val327=
XM_017026537.1:c.979G=	XP_016882026.1:p.Val327=
XM_024451434.1:c.931G=	XP_024307202.1:p.Val311=