Canonical Allele Identifier: CA2668968249

Gene: KNG1

Linked Data

• gnomAD v4: 3-186742061-T-TGTAACA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186742064_186742069dup , CM000665.2:g.186742064_186742069dup	GRCh38
NC_000003.11:g.186459853_186459858dup , CM000665.1:g.186459853_186459858dup	GRCh37
NC_000003.10:g.187942547_187942552dup	NCBI36
NG_016009.1:g.29756_29761dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287611.8:c.1203+465_1203+470dup	ENSP00000287611.2:n.1203+465_1203+470dup
ENST00000644859.2:c.1668_1673dup MANE Select	ENSP00000493985.1:p.Val558_Thr559insThrVal
ENST00000265023.8:c.1668_1673dup	ENSP00000265023.4:p.Val558_Thr559insThrVal
ENST00000287611.6:c.1203+465_1203+470dup	ENSP00000287611.2:n.1203+465_1203+470dup
ENST00000447445.1:c.1095+465_1095+470dup	ENSP00000396025.1:n.1095+465_1095+470dup
NM_000893.3:c.1203+465_1203+470dup	NP_000884.1:n.1203+465_1203+470dup
NM_001102416.2:c.1668_1673dup	NP_001095886.1:p.Val558_Thr559insThrVal
NM_001166451.1:c.1095+465_1095+470dup	NP_001159923.1:n.1095+465_1095+470dup
NM_000893.4:c.1203+465_1203+470dup	NP_000884.1:n.1203+465_1203+470dup
NM_001102416.3:c.1668_1673dup MANE Select	NP_001095886.1:p.Val558_Thr559insThrVal
NM_001166451.2:c.1095+465_1095+470dup	NP_001159923.1:n.1095+465_1095+470dup