Canonical Allele Identifier: CA1427067369
Gene: KNG1 HGNC NCBI

Linked Data

dbSNP Id: rs1720670859

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186736405T>G , CM000665.2:g.186736405T>G GRCh38
NC_000003.11:g.186454194T>G , CM000665.1:g.186454194T>G GRCh37
NC_000003.10:g.187936888T>G NCBI36
NG_016009.1:g.24097T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287611.8:c.931-2694T>G ENSP00000287611.2:n.931-2694T>G
ENST00000644859.2:c.931-2694T>G MANE Select ENSP00000493985.1:n.931-2694T>G
ENST00000265023.8:c.931-2694T>G ENSP00000265023.4:n.931-2694T>G
ENST00000287611.6:c.931-2694T>G ENSP00000287611.2:n.931-2694T>G
ENST00000447445.1:c.823-2694T>G ENSP00000396025.1:n.823-2694T>G
NM_000893.3:c.931-2694T>G NP_000884.1:n.931-2694T>G
NM_001102416.2:c.931-2694T>G NP_001095886.1:n.931-2694T>G
NM_001166451.1:c.823-2694T>G NP_001159923.1:n.823-2694T>G
NM_000893.4:c.931-2694T>G NP_000884.1:n.931-2694T>G
NM_001102416.3:c.931-2694T>G MANE Select NP_001095886.1:n.931-2694T>G
NM_001166451.2:c.823-2694T>G NP_001159923.1:n.823-2694T>G