Canonical Allele Identifier: CA355733595

Gene: KNG1

Linked Data

• dbSNP Id: rs2108638372
• MyVariant Identifiers: chr3:g.186459827A>G (hg19) ; chr3:g.186742038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186742038A>G , CM000665.2:g.186742038A>G	GRCh38
NC_000003.11:g.186459827A>G , CM000665.1:g.186459827A>G	GRCh37
NC_000003.10:g.187942521A>G	NCBI36
NG_016009.1:g.29730A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287611.8:c.1203+439A>G	ENSP00000287611.2:n.1203+439A>G
ENST00000644859.2:c.1642A>G MANE Select	ENSP00000493985.1:p.Ile548Val
ENST00000265023.8:c.1642A>G	ENSP00000265023.4:p.Ile548Val
ENST00000287611.6:c.1203+439A>G	ENSP00000287611.2:n.1203+439A>G
ENST00000447445.1:c.1095+439A>G	ENSP00000396025.1:n.1095+439A>G
NM_000893.3:c.1203+439A>G	NP_000884.1:n.1203+439A>G
NM_001102416.2:c.1642A>G	NP_001095886.1:p.Ile548Val
NM_001166451.1:c.1095+439A>G	NP_001159923.1:n.1095+439A>G
NM_000893.4:c.1203+439A>G	NP_000884.1:n.1203+439A>G
NM_001102416.3:c.1642A>G MANE Select	NP_001095886.1:p.Ile548Val
NM_001166451.2:c.1095+439A>G	NP_001159923.1:n.1095+439A>G