Canonical Allele Identifier: CA2668967235
Gene: KNG1 HGNC NCBI

Linked Data

gnomAD v4: 3-186736401-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186736401T>C , CM000665.2:g.186736401T>C GRCh38
NC_000003.11:g.186454190T>C , CM000665.1:g.186454190T>C GRCh37
NC_000003.10:g.187936884T>C NCBI36
NG_016009.1:g.24093T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287611.8:c.931-2698T>C ENSP00000287611.2:n.931-2698T>C
ENST00000644859.2:c.931-2698T>C MANE Select ENSP00000493985.1:n.931-2698T>C
ENST00000265023.8:c.931-2698T>C ENSP00000265023.4:n.931-2698T>C
ENST00000287611.6:c.931-2698T>C ENSP00000287611.2:n.931-2698T>C
ENST00000447445.1:c.823-2698T>C ENSP00000396025.1:n.823-2698T>C
NM_000893.3:c.931-2698T>C NP_000884.1:n.931-2698T>C
NM_001102416.2:c.931-2698T>C NP_001095886.1:n.931-2698T>C
NM_001166451.1:c.823-2698T>C NP_001159923.1:n.823-2698T>C
NM_000893.4:c.931-2698T>C NP_000884.1:n.931-2698T>C
NM_001102416.3:c.931-2698T>C MANE Select NP_001095886.1:n.931-2698T>C
NM_001166451.2:c.823-2698T>C NP_001159923.1:n.823-2698T>C
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