Canonical Allele Identifier: CA212727611

Gene: CRTAC1

Linked Data

• dbSNP Id: rs1005716774
• MyVariant Identifiers: chr10:g.99637616T>C (hg19) ; chr10:g.97877859T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97877859T>C , CM000672.2:g.97877859T>C	GRCh38
NC_000010.10:g.99637616T>C , CM000672.1:g.99637616T>C	GRCh37
NC_000010.9:g.99627606T>C	NCBI36
NG_029831.1:g.157970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370597.8:c.1819+2390A>G MANE Select	ENSP00000359629.3:n.1819+2390A>G
ENST00000370597.7:c.1819+2390A>G	ENSP00000359629.3:n.1819+2390A>G
ENST00000413387.5:c.1464+2390A>G	ENSP00000408445.1:n.1464+2390A>G
NM_018058.6:c.1819+2390A>G	NP_060528.3:n.1819+2390A>G
XM_011539917.1:c.1819+2390A>G	XP_011538219.1:n.1819+2390A>G
XM_017016366.1:c.1819+2390A>G	XP_016871855.1:n.1819+2390A>G
XM_017016367.1:c.1819+2390A>G	XP_016871856.1:n.1819+2390A>G
NM_018058.7:c.1819+2390A>G MANE Select	NP_060528.3:n.1819+2390A>G