Canonical Allele Identifier: CA212727602

Gene: CRTAC1

Linked Data

• dbSNP Id: rs556931311
• gnomAD v2: 10-99637581-A-C
• gnomAD v3: 10-97877824-A-C
• gnomAD v4: 10-97877824-A-C
• MyVariant Identifiers: chr10:g.99637581A>C (hg19) ; chr10:g.97877824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97877824A>C , CM000672.2:g.97877824A>C	GRCh38
NC_000010.10:g.99637581A>C , CM000672.1:g.99637581A>C	GRCh37
NC_000010.9:g.99627571A>C	NCBI36
NG_029831.1:g.158005T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370597.8:c.1819+2425T>G MANE Select	ENSP00000359629.3:n.1819+2425T>G
ENST00000370597.7:c.1819+2425T>G	ENSP00000359629.3:n.1819+2425T>G
ENST00000413387.5:c.1464+2425T>G	ENSP00000408445.1:n.1464+2425T>G
NM_018058.6:c.1819+2425T>G	NP_060528.3:n.1819+2425T>G
XM_011539917.1:c.1819+2425T>G	XP_011538219.1:n.1819+2425T>G
XM_017016366.1:c.1819+2425T>G	XP_016871855.1:n.1819+2425T>G
XM_017016367.1:c.1819+2425T>G	XP_016871856.1:n.1819+2425T>G
NM_018058.7:c.1819+2425T>G MANE Select	NP_060528.3:n.1819+2425T>G