Canonical Allele Identifier: CA1583175222
Community Standard Title: NC_000005.10:g.132448701G=

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132448701G= , CM000667.2:g.132448701G= GRCh38
NC_000005.9:g.131784393G= , CM000667.1:g.131784393G= GRCh37
NC_000005.8:g.131812292G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001207001.2:c.49-949G= (CARINH) NP_001193930.1:n.49-949G=
NR_045116.1:n.388-949G= (CARINH)
NR_161242.1:n.232-949G= (CARINH)
ENST00000337752.6:c.49-949G= (CARINH) ENSP00000338228.2:n.49-949G=
ENST00000378947.7:c.49-949G= (CARINH) ENSP00000368230.3:n.49-949G=
ENST00000378953.8:c.49-949G= (CARINH) ENSP00000368236.4:n.49-949G=
ENST00000407797.5:c.49-949G= (CARINH) ENSP00000385513.1:n.49-949G=
ENST00000461203.5:n.180-949G= (CARINH)
ENST00000621237.1:c.49-949G= (CARINH) ENSP00000481774.1:n.49-949G=
ENST00000638452.2:c.-208-949G= ENSP00000492349.2:n.-208-949G=
ENST00000638504.1:n.206+28761G=
ENST00000638568.2:c.-350-949G= ENSP00000491158.2:n.-350-949G=
ENST00000639899.1:n.250-949G=
ENST00000679921.1:c.*73+846C= (IRF1) ENSP00000505766.1:n.*73+846C=