Canonical Allele Identifier: CA1591154495

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150899025C= , CM000667.2:g.150899025C= GRCh38
NC_000005.9:g.150278587C= , CM000667.1:g.150278587C= GRCh37
NC_000005.8:g.150258780C= NCBI36
NG_016866.1:g.10959G=
NG_027809.2:g.57503C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446148.7:c.16-471G= (ZNF300) ENSP00000397178.3:n.16-471G=
ENST00000274599.10:c.16-471G= (ZNF300) MANE Select ENSP00000274599.5:n.16-471G=
ENST00000274599.9:c.16-471G= (ZNF300) ENSP00000274599.5:n.16-471G=
ENST00000394226.2:c.16-471G= (ZNF300) ENSP00000377773.2:n.16-471G=
ENST00000418587.6:c.-93-471G= (ZNF300) ENSP00000392593.2:n.-93-471G=
ENST00000427179.5:c.16-471G= (ZNF300) ENSP00000414195.1:n.16-471G=
ENST00000446148.6:c.64-471G= (ZNF300) ENSP00000397178.2:n.64-471G=
ENST00000520549.1:c.356-1564C= (IRGM)
NM_001172831.1:c.64-471G= (ZNF300) NP_001166302.1:n.64-471G=
NM_001172832.1:c.-93-471G= (ZNF300) NP_001166303.1:n.-93-471G=
NM_052860.2:c.16-471G= (ZNF300) NP_443092.1:n.16-471G=
XM_006714806.1:c.16-471G= (ZNF300) XP_006714869.1:n.16-471G=
XM_011537641.1:c.594-1564C= (IRGM) XP_011535943.1:n.594-1564C=
XM_011537702.1:c.31-471G= (ZNF300) XP_011536004.1:n.31-471G=
XM_011537703.1:c.31-471G= (ZNF300) XP_011536005.1:n.31-471G=
XR_944324.1:n.165-1564C= (IRGM)
NM_001346557.1:c.594-1564C= (IRGM) NP_001333486.1:n.594-1564C=
XM_011537702.2:c.31-471G= (ZNF300) XP_011536004.1:n.31-471G=
NM_001346557.2:c.594-1564C= (IRGM) NP_001333486.1:n.594-1564C=
NM_001172831.3:c.64-471G= (ZNF300) NP_001166302.1:n.64-471G=
NM_001172832.3:c.-93-471G= (ZNF300) NP_001166303.1:n.-93-471G=
NM_052860.4:c.16-471G= (ZNF300) MANE Select NP_443092.1:n.16-471G=
NR_170598.1:n.1844-1564C= (IRGM)