Canonical Allele Identifier: CA2583620220

Gene: CRTC1

Linked Data

• gnomAD v4: 19-18781934-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18781934A>G , CM000681.2:g.18781934A>G	GRCh38
NC_000019.9:g.18892744A>G , CM000681.1:g.18892744A>G	GRCh37
NC_000019.8:g.18753744A>G	NCBI36
NG_007070.1:g.14371T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000321949.13:c.*4552A>G MANE Select	ENSP00000323332.7:n.*4552A>G
ENST00000338797.10:c.*4552A>G	ENSP00000345001.5:n.*4552A>G
NM_001098482.1:c.*4552A>G	NP_001091952.1:n.*4552A>G
NM_015321.2:c.*4552A>G	NP_056136.2:n.*4552A>G
XM_005259833.2:c.*4552A>G	XP_005259890.1:n.*4552A>G
XM_005259834.1:c.*4552A>G	XP_005259891.1:n.*4552A>G
XM_005259835.2:c.*4552A>G	XP_005259892.1:n.*4552A>G
XM_005259836.2:c.*4552A>G	XP_005259893.1:n.*4552A>G
XM_006722710.2:c.*4552A>G	XP_006722773.1:n.*4552A>G
XM_011527842.1:c.*4552A>G	XP_011526144.1:n.*4552A>G
XM_005259833.3:c.*4552A>G	XP_005259890.1:n.*4552A>G
XM_005259835.3:c.*4552A>G	XP_005259892.1:n.*4552A>G
XM_005259836.3:c.*4552A>G	XP_005259893.1:n.*4552A>G
XM_006722710.3:c.*4552A>G	XP_006722773.1:n.*4552A>G
XM_011527842.3:c.*4552A>G	XP_011526144.1:n.*4552A>G
XM_024451434.1:c.*4552A>G	XP_024307202.1:n.*4552A>G
NM_015321.3:c.*4552A>G MANE Select	NP_056136.2:n.*4552A>G
NM_001098482.2:c.*4552A>G	NP_001091952.1:n.*4552A>G