Canonical Allele Identifier: CA384148447

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209866-G-T
• MyVariant Identifiers: chr12:g.25362800G>T (hg19) ; chr12:g.25209866G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209866G>T , CM000674.2:g.25209866G>T	GRCh38
NC_000012.11:g.25362800G>T , CM000674.1:g.25362800G>T	GRCh37
NC_000012.10:g.25254067G>T	NCBI36
NG_007524.1:g.46055C>A
NG_007524.2:g.46138C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.157C>A	ENSP00000452512.1:p.His53Asn
ENST00000685328.1:c.496C>A	ENSP00000508921.1:p.His166Asn
ENST00000686877.1:c.*467C>A	ENSP00000510431.1:n.*467C>A
ENST00000687356.1:c.*194C>A	ENSP00000510511.1:n.*194C>A
ENST00000688228.1:n.970C>A
ENST00000688940.1:c.496C>A	ENSP00000509238.1:p.His166Asn
ENST00000690406.1:c.299C>A
ENST00000690804.1:c.*457C>A	ENSP00000508568.1:n.*457C>A
ENST00000692768.1:c.298C>A	ENSP00000510254.1:p.His100Asn
ENST00000693229.1:c.421C>A	ENSP00000509223.1:p.His141Asn
ENST00000256078.10:c.*50C>A MANE Plus Clinical	ENSP00000256078.5:n.*50C>A
ENST00000311936.8:c.496C>A MANE Select	ENSP00000308495.3:p.His166Asn
ENST00000256078.8:c.*50C>A	ENSP00000256078.4:n.*50C>A
ENST00000311936.7:c.496C>A	ENSP00000308495.3:p.His166Asn
ENST00000557334.5:c.157C>A	ENSP00000452512.1:p.His53Asn
NM_004985.4:c.496C>A	NP_004976.2:p.His166Asn
NM_033360.3:c.*50C>A	NP_203524.1:n.*50C>A
XM_006719069.2:c.*50C>A	XP_006719132.1:n.*50C>A
XM_011520653.1:c.496C>A	XP_011518955.1:p.His166Asn
XM_006719069.4:c.*50C>A	XP_006719132.1:n.*50C>A
XM_011520653.3:c.496C>A	XP_011518955.1:p.His166Asn
NM_001369786.1:c.*50C>A	NP_001356715.1:n.*50C>A
NM_001369787.1:c.496C>A	NP_001356716.1:p.His166Asn
NM_004985.5:c.496C>A MANE Select	NP_004976.2:p.His166Asn
NM_033360.4:c.*50C>A MANE Plus Clinical	NP_203524.1:n.*50C>A