Canonical Allele Identifier: CA404866754

Gene: CRTC1

Linked Data

• MyVariant Identifiers: chr19:g.18876318C>A (hg19) ; chr19:g.18765508C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18765508C>A , CM000681.2:g.18765508C>A	GRCh38
NC_000019.9:g.18876318C>A , CM000681.1:g.18876318C>A	GRCh37
NC_000019.8:g.18737318C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321949.13:c.991C>A MANE Select	ENSP00000323332.7:p.Pro331Thr
ENST00000321949.12:c.991C>A	ENSP00000323332.7:p.Pro331Thr
ENST00000338797.10:c.1039C>A	ENSP00000345001.5:p.Pro347Thr
ENST00000594658.5:c.868C>A	ENSP00000468893.1:p.Pro290Thr
ENST00000601916.1:c.766C>A	ENSP00000469285.1:p.Pro256Thr
NM_001098482.1:c.1039C>A	NP_001091952.1:p.Pro347Thr
NM_015321.2:c.991C>A	NP_056136.2:p.Pro331Thr
XM_005259833.2:c.1039C>A	XP_005259890.1:p.Pro347Thr
XM_005259834.1:c.991C>A	XP_005259891.1:p.Pro331Thr
XM_005259835.2:c.1039C>A	XP_005259892.1:p.Pro347Thr
XM_005259836.2:c.1039C>A	XP_005259893.1:p.Pro347Thr
XM_006722710.2:c.1039C>A	XP_006722773.1:p.Pro347Thr
XM_011527842.1:c.1039C>A	XP_011526144.1:p.Pro347Thr
XM_005259833.3:c.1039C>A	XP_005259890.1:p.Pro347Thr
XM_005259835.3:c.1039C>A	XP_005259892.1:p.Pro347Thr
XM_005259836.3:c.1039C>A	XP_005259893.1:p.Pro347Thr
XM_006722710.3:c.1039C>A	XP_006722773.1:p.Pro347Thr
XM_011527842.3:c.1039C>A	XP_011526144.1:p.Pro347Thr
XM_017026536.1:c.1039C>A	XP_016882025.1:p.Pro347Thr
XM_017026537.1:c.1039C>A	XP_016882026.1:p.Pro347Thr
XM_024451434.1:c.991C>A	XP_024307202.1:p.Pro331Thr
NM_015321.3:c.991C>A MANE Select	NP_056136.2:p.Pro331Thr
NM_001098482.2:c.1039C>A	NP_001091952.1:p.Pro347Thr