Canonical Allele Identifier: CA355733613

Gene: KNG1

Linked Data

• MyVariant Identifiers: chr3:g.186459830C>G (hg19) ; chr3:g.186742041C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186742041C>G , CM000665.2:g.186742041C>G	GRCh38
NC_000003.11:g.186459830C>G , CM000665.1:g.186459830C>G	GRCh37
NC_000003.10:g.187942524C>G	NCBI36
NG_016009.1:g.29733C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000287611.8:c.1203+442C>G	ENSP00000287611.2:n.1203+442C>G
ENST00000644859.2:c.1645C>G MANE Select	ENSP00000493985.1:p.Pro549Ala
ENST00000265023.8:c.1645C>G	ENSP00000265023.4:p.Pro549Ala
ENST00000287611.6:c.1203+442C>G	ENSP00000287611.2:n.1203+442C>G
ENST00000447445.1:c.1095+442C>G	ENSP00000396025.1:n.1095+442C>G
NM_000893.3:c.1203+442C>G	NP_000884.1:n.1203+442C>G
NM_001102416.2:c.1645C>G	NP_001095886.1:p.Pro549Ala
NM_001166451.1:c.1095+442C>G	NP_001159923.1:n.1095+442C>G
NM_000893.4:c.1203+442C>G	NP_000884.1:n.1203+442C>G
NM_001102416.3:c.1645C>G MANE Select	NP_001095886.1:p.Pro549Ala
NM_001166451.2:c.1095+442C>G	NP_001159923.1:n.1095+442C>G