Canonical Allele Identifier: CA1140064194
Community Standard Title: NM_018240.7(KIRREL1):c.917-8C=
Gene: KIRREL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158088319C= , CM000663.2:g.158088319C= GRCh38
NC_000001.10:g.158058109C= , CM000663.1:g.158058109C= GRCh37
NC_000001.9:g.156324733C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_018240.7:c.917-8C= MANE Select NP_060710.3:n.917-8C=
ENST00000359209.11:c.917-8C= MANE Select ENSP00000352138.6:n.917-8C=
NM_001286349.1:c.617-8C= NP_001273278.1:n.617-8C=
NM_001286349.2:c.617-8C= NP_001273278.1:n.617-8C=
NM_018240.6:c.917-8C= NP_060710.3:n.917-8C=
ENST00000359209.10:c.917-8C= ENSP00000352138.6:n.917-8C=
ENST00000360089.8:c.425-8C= ENSP00000353202.4:n.425-8C=
ENST00000368172.1:c.311-8C= ENSP00000357154.1:n.311-8C=
ENST00000368172.2:c.565-8C=
ENST00000368173.7:c.617-8C= ENSP00000357155.4:n.617-8C=
XM_005245305.3:c.917-8C= XP_005245362.1:n.917-8C=
XM_005245305.5:c.917-8C= XP_005245362.1:n.917-8C=
XM_011509716.1:c.734-8C= XP_011508018.1:n.734-8C=