Canonical Allele Identifier: CA2580598927
Gene: CRTAC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97877821G>T , CM000672.2:g.97877821G>T GRCh38
NC_000010.10:g.99637578G>T , CM000672.1:g.99637578G>T GRCh37
NC_000010.9:g.99627568G>T NCBI36
NG_029831.1:g.158008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370597.8:c.1819+2428C>A MANE Select ENSP00000359629.3:n.1819+2428C>A
ENST00000370597.7:c.1819+2428C>A ENSP00000359629.3:n.1819+2428C>A
ENST00000413387.5:c.1464+2428C>A ENSP00000408445.1:n.1464+2428C>A
NM_018058.6:c.1819+2428C>A NP_060528.3:n.1819+2428C>A
XM_011539917.1:c.1819+2428C>A XP_011538219.1:n.1819+2428C>A
XM_017016366.1:c.1819+2428C>A XP_016871855.1:n.1819+2428C>A
XM_017016367.1:c.1819+2428C>A XP_016871856.1:n.1819+2428C>A
NM_018058.7:c.1819+2428C>A MANE Select NP_060528.3:n.1819+2428C>A
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