Canonical Allele Identifier: CA384148492

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209887-A-C
• MyVariant Identifiers: chr12:g.25362821A>C (hg19) ; chr12:g.25209887A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209887A>C , CM000674.2:g.25209887A>C	GRCh38
NC_000012.11:g.25362821A>C , CM000674.1:g.25362821A>C	GRCh37
NC_000012.10:g.25254088A>C	NCBI36
NG_007524.1:g.46034T>G
NG_007524.2:g.46117T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.136T>G	ENSP00000452512.1:p.Leu46Val
ENST00000685328.1:c.475T>G	ENSP00000508921.1:p.Leu159Val
ENST00000686877.1:c.*446T>G	ENSP00000510431.1:n.*446T>G
ENST00000687356.1:c.*173T>G	ENSP00000510511.1:n.*173T>G
ENST00000688228.1:n.949T>G
ENST00000688940.1:c.475T>G	ENSP00000509238.1:p.Leu159Val
ENST00000690406.1:c.278T>G
ENST00000690804.1:c.*436T>G	ENSP00000508568.1:n.*436T>G
ENST00000692768.1:c.277T>G	ENSP00000510254.1:p.Leu93Val
ENST00000693229.1:c.400T>G	ENSP00000509223.1:p.Leu134Val
ENST00000256078.10:c.*29T>G MANE Plus Clinical	ENSP00000256078.5:n.*29T>G
ENST00000311936.8:c.475T>G MANE Select	ENSP00000308495.3:p.Leu159Val
ENST00000256078.8:c.*29T>G	ENSP00000256078.4:n.*29T>G
ENST00000311936.7:c.475T>G	ENSP00000308495.3:p.Leu159Val
ENST00000557334.5:c.136T>G	ENSP00000452512.1:p.Leu46Val
NM_004985.4:c.475T>G	NP_004976.2:p.Leu159Val
NM_033360.3:c.*29T>G	NP_203524.1:n.*29T>G
XM_006719069.2:c.*29T>G	XP_006719132.1:n.*29T>G
XM_011520653.1:c.475T>G	XP_011518955.1:p.Leu159Val
XM_006719069.4:c.*29T>G	XP_006719132.1:n.*29T>G
XM_011520653.3:c.475T>G	XP_011518955.1:p.Leu159Val
NM_001369786.1:c.*29T>G	NP_001356715.1:n.*29T>G
NM_001369787.1:c.475T>G	NP_001356716.1:p.Leu159Val
NM_004985.5:c.475T>G MANE Select	NP_004976.2:p.Leu159Val
NM_033360.4:c.*29T>G MANE Plus Clinical	NP_203524.1:n.*29T>G