Canonical Allele Identifier: CA1930623861
Gene: CRTAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97877748C= , CM000672.2:g.97877748C= GRCh38
NC_000010.10:g.99637505C= , CM000672.1:g.99637505C= GRCh37
NC_000010.9:g.99627495C= NCBI36
NG_029831.1:g.158081G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370597.8:c.1819+2501G= MANE Select ENSP00000359629.3:n.1819+2501G=
ENST00000370597.7:c.1819+2501G= ENSP00000359629.3:n.1819+2501G=
ENST00000413387.5:c.1464+2501G= ENSP00000408445.1:n.1464+2501G=
NM_018058.6:c.1819+2501G= NP_060528.3:n.1819+2501G=
XM_011539917.1:c.1819+2501G= XP_011538219.1:n.1819+2501G=
XM_017016366.1:c.1819+2501G= XP_016871855.1:n.1819+2501G=
XM_017016367.1:c.1819+2501G= XP_016871856.1:n.1819+2501G=
NM_018058.7:c.1819+2501G= MANE Select NP_060528.3:n.1819+2501G=