Canonical Allele Identifier: CA2668966372

Gene: KNG1

Linked Data

• gnomAD v4: 3-186718618-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186718618A>C , CM000665.2:g.186718618A>C	GRCh38
NC_000003.11:g.186436407A>C , CM000665.1:g.186436407A>C	GRCh37
NC_000003.10:g.187919101A>C	NCBI36
NG_016009.1:g.6310A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000287611.8:c.195+881A>C	ENSP00000287611.2:n.195+881A>C
ENST00000644859.2:c.195+881A>C MANE Select	ENSP00000493985.1:n.195+881A>C
ENST00000645544.1:n.338+881A>C
ENST00000265023.8:c.195+881A>C	ENSP00000265023.4:n.195+881A>C
ENST00000287611.6:c.195+881A>C	ENSP00000287611.2:n.195+881A>C
ENST00000447445.1:c.195+881A>C	ENSP00000396025.1:n.195+881A>C
NM_000893.3:c.195+881A>C	NP_000884.1:n.195+881A>C
NM_001102416.2:c.195+881A>C	NP_001095886.1:n.195+881A>C
NM_001166451.1:c.195+881A>C	NP_001159923.1:n.195+881A>C
NM_000893.4:c.195+881A>C	NP_000884.1:n.195+881A>C
NM_001102416.3:c.195+881A>C MANE Select	NP_001095886.1:n.195+881A>C
NM_001166451.2:c.195+881A>C	NP_001159923.1:n.195+881A>C