Canonical Allele Identifier: CA1427067347
Gene: KNG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186736367A= , CM000665.2:g.186736367A= GRCh38
NC_000003.11:g.186454156A= , CM000665.1:g.186454156A= GRCh37
NC_000003.10:g.187936850A= NCBI36
NG_016009.1:g.24059A=

Transcript Alleles

HGVS Amino-acid change
ENST00000287611.8:c.931-2732A= ENSP00000287611.2:n.931-2732A=
ENST00000644859.2:c.931-2732A= MANE Select ENSP00000493985.1:n.931-2732A=
ENST00000265023.8:c.931-2732A= ENSP00000265023.4:n.931-2732A=
ENST00000287611.6:c.931-2732A= ENSP00000287611.2:n.931-2732A=
ENST00000447445.1:c.823-2732A= ENSP00000396025.1:n.823-2732A=
NM_000893.3:c.931-2732A= NP_000884.1:n.931-2732A=
NM_001102416.2:c.931-2732A= NP_001095886.1:n.931-2732A=
NM_001166451.1:c.823-2732A= NP_001159923.1:n.823-2732A=
NM_000893.4:c.931-2732A= NP_000884.1:n.931-2732A=
NM_001102416.3:c.931-2732A= MANE Select NP_001095886.1:n.931-2732A=
NM_001166451.2:c.823-2732A= NP_001159923.1:n.823-2732A=