Canonical Allele Identifier: CA212727607
Gene: CRTAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1034294967
MyVariant Identifiers: chr10:g.99637609G>C (hg19) chr10:g.97877852G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97877852G>C , CM000672.2:g.97877852G>C GRCh38
NC_000010.10:g.99637609G>C , CM000672.1:g.99637609G>C GRCh37
NC_000010.9:g.99627599G>C NCBI36
NG_029831.1:g.157977C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370597.8:c.1819+2397C>G MANE Select ENSP00000359629.3:n.1819+2397C>G
ENST00000370597.7:c.1819+2397C>G ENSP00000359629.3:n.1819+2397C>G
ENST00000413387.5:c.1464+2397C>G ENSP00000408445.1:n.1464+2397C>G
NM_018058.6:c.1819+2397C>G NP_060528.3:n.1819+2397C>G
XM_011539917.1:c.1819+2397C>G XP_011538219.1:n.1819+2397C>G
XM_017016366.1:c.1819+2397C>G XP_016871855.1:n.1819+2397C>G
XM_017016367.1:c.1819+2397C>G XP_016871856.1:n.1819+2397C>G
NM_018058.7:c.1819+2397C>G MANE Select NP_060528.3:n.1819+2397C>G
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