Canonical Allele Identifier: CA1427079362
Gene: KNG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186718615C= , CM000665.2:g.186718615C= GRCh38
NC_000003.11:g.186436404C= , CM000665.1:g.186436404C= GRCh37
NC_000003.10:g.187919098C= NCBI36
NG_016009.1:g.6307C=

Transcript Alleles

HGVS Amino-acid change
ENST00000287611.8:c.195+878C= ENSP00000287611.2:n.195+878C=
ENST00000644859.2:c.195+878C= MANE Select ENSP00000493985.1:n.195+878C=
ENST00000645544.1:n.338+878C=
ENST00000265023.8:c.195+878C= ENSP00000265023.4:n.195+878C=
ENST00000287611.6:c.195+878C= ENSP00000287611.2:n.195+878C=
ENST00000447445.1:c.195+878C= ENSP00000396025.1:n.195+878C=
NM_000893.3:c.195+878C= NP_000884.1:n.195+878C=
NM_001102416.2:c.195+878C= NP_001095886.1:n.195+878C=
NM_001166451.1:c.195+878C= NP_001159923.1:n.195+878C=
NM_000893.4:c.195+878C= NP_000884.1:n.195+878C=
NM_001102416.3:c.195+878C= MANE Select NP_001095886.1:n.195+878C=
NM_001166451.2:c.195+878C= NP_001159923.1:n.195+878C=