Canonical Allele Identifier: CA783944629

Gene: CRTC1

Linked Data

• dbSNP Id: rs1196494026
• MyVariant Identifiers: chr19:g.18803177C>G (hg19) ; chr19:g.18692367C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18692367C>G , CM000681.2:g.18692367C>G	GRCh38
NC_000019.9:g.18803177C>G , CM000681.1:g.18803177C>G	GRCh37
NC_000019.8:g.18664177C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321949.13:c.126+8539C>G MANE Select	ENSP00000323332.7:n.126+8539C>G
ENST00000321949.12:c.126+8539C>G	ENSP00000323332.7:n.126+8539C>G
ENST00000338797.10:c.126+8539C>G	ENSP00000345001.5:n.126+8539C>G
NM_001098482.1:c.126+8539C>G	NP_001091952.1:n.126+8539C>G
NM_015321.2:c.126+8539C>G	NP_056136.2:n.126+8539C>G
XM_005259833.2:c.126+8539C>G	XP_005259890.1:n.126+8539C>G
XM_005259834.1:c.126+8539C>G	XP_005259891.1:n.126+8539C>G
XM_005259835.2:c.126+8539C>G	XP_005259892.1:n.126+8539C>G
XM_005259836.2:c.126+8539C>G	XP_005259893.1:n.126+8539C>G
XM_006722710.2:c.126+8539C>G	XP_006722773.1:n.126+8539C>G
XM_011527842.1:c.126+8539C>G	XP_011526144.1:n.126+8539C>G
XM_005259833.3:c.126+8539C>G	XP_005259890.1:n.126+8539C>G
XM_005259835.3:c.126+8539C>G	XP_005259892.1:n.126+8539C>G
XM_005259836.3:c.126+8539C>G	XP_005259893.1:n.126+8539C>G
XM_006722710.3:c.126+8539C>G	XP_006722773.1:n.126+8539C>G
XM_011527842.3:c.126+8539C>G	XP_011526144.1:n.126+8539C>G
XM_017026536.1:c.126+8539C>G	XP_016882025.1:n.126+8539C>G
XM_017026537.1:c.126+8539C>G	XP_016882026.1:n.126+8539C>G
XM_017026538.2:c.126+8539C>G	XP_016882027.1:n.126+8539C>G
XM_024451434.1:c.126+8539C>G	XP_024307202.1:n.126+8539C>G
NM_015321.3:c.126+8539C>G MANE Select	NP_056136.2:n.126+8539C>G
NM_001098482.2:c.126+8539C>G	NP_001091952.1:n.126+8539C>G