Canonical Allele Identifier: CA11562680

Gene: KNG1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186733447T>C , CM000665.2:g.186733447T>C	GRCh38
NC_000003.11:g.186451236T>C , CM000665.1:g.186451236T>C	GRCh37
NC_000003.10:g.187933930T>C	NCBI36
NG_016009.1:g.21139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287611.8:c.930+773T>C	ENSP00000287611.2:n.930+773T>C
ENST00000644859.2:c.930+773T>C MANE Select	ENSP00000493985.1:n.930+773T>C
ENST00000265023.8:c.930+773T>C	ENSP00000265023.4:n.930+773T>C
ENST00000287611.6:c.930+773T>C	ENSP00000287611.2:n.930+773T>C
ENST00000447445.1:c.822+773T>C	ENSP00000396025.1:n.822+773T>C
NM_000893.3:c.930+773T>C	NP_000884.1:n.930+773T>C
NM_001102416.2:c.930+773T>C	NP_001095886.1:n.930+773T>C
NM_001166451.1:c.822+773T>C	NP_001159923.1:n.822+773T>C
NM_000893.4:c.930+773T>C	NP_000884.1:n.930+773T>C
NM_001102416.3:c.930+773T>C MANE Select	NP_001095886.1:n.930+773T>C
NM_001166451.2:c.822+773T>C	NP_001159923.1:n.822+773T>C