Canonical Allele Identifier: CA404866756

Gene: CRTC1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321949.13:c.991C>G MANE Select	ENSP00000323332.7:p.Pro331Ala
ENST00000321949.12:c.991C>G	ENSP00000323332.7:p.Pro331Ala
ENST00000338797.10:c.1039C>G	ENSP00000345001.5:p.Pro347Ala
ENST00000594658.5:c.868C>G	ENSP00000468893.1:p.Pro290Ala
ENST00000601916.1:c.766C>G	ENSP00000469285.1:p.Pro256Ala
NM_001098482.1:c.1039C>G	NP_001091952.1:p.Pro347Ala
NM_015321.2:c.991C>G	NP_056136.2:p.Pro331Ala
XM_005259833.2:c.1039C>G	XP_005259890.1:p.Pro347Ala
XM_005259834.1:c.991C>G	XP_005259891.1:p.Pro331Ala
XM_005259835.2:c.1039C>G	XP_005259892.1:p.Pro347Ala
XM_005259836.2:c.1039C>G	XP_005259893.1:p.Pro347Ala
XM_006722710.2:c.1039C>G	XP_006722773.1:p.Pro347Ala
XM_011527842.1:c.1039C>G	XP_011526144.1:p.Pro347Ala
XM_005259833.3:c.1039C>G	XP_005259890.1:p.Pro347Ala
XM_005259835.3:c.1039C>G	XP_005259892.1:p.Pro347Ala
XM_005259836.3:c.1039C>G	XP_005259893.1:p.Pro347Ala
XM_006722710.3:c.1039C>G	XP_006722773.1:p.Pro347Ala
XM_011527842.3:c.1039C>G	XP_011526144.1:p.Pro347Ala
XM_017026536.1:c.1039C>G	XP_016882025.1:p.Pro347Ala
XM_017026537.1:c.1039C>G	XP_016882026.1:p.Pro347Ala
XM_024451434.1:c.991C>G	XP_024307202.1:p.Pro331Ala
NM_015321.3:c.991C>G MANE Select	NP_056136.2:p.Pro331Ala
NM_001098482.2:c.1039C>G	NP_001091952.1:p.Pro347Ala