Canonical Allele Identifier: CA2617994272

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209716-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209716C>A , CM000674.2:g.25209716C>A	GRCh38
NC_000012.11:g.25362650C>A , CM000674.1:g.25362650C>A	GRCh37
NC_000012.10:g.25253917C>A	NCBI36
NG_007524.1:g.46205G>T
NG_007524.2:g.46288G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*79G>T	ENSP00000452512.1:n.*79G>T
ENST00000685328.1:c.*79G>T	ENSP00000508921.1:n.*79G>T
ENST00000686877.1:c.*617G>T	ENSP00000510431.1:n.*617G>T
ENST00000687356.1:c.*344G>T	ENSP00000510511.1:n.*344G>T
ENST00000688228.1:n.1120G>T
ENST00000688940.1:c.*79G>T	ENSP00000509238.1:n.*79G>T
ENST00000690406.1:c.449G>T
ENST00000690804.1:c.*607G>T	ENSP00000508568.1:n.*607G>T
ENST00000692768.1:c.*79G>T	ENSP00000510254.1:n.*79G>T
ENST00000693229.1:c.*79G>T	ENSP00000509223.1:n.*79G>T
ENST00000256078.10:c.*200G>T MANE Plus Clinical	ENSP00000256078.5:n.*200G>T
ENST00000311936.8:c.*79G>T MANE Select	ENSP00000308495.3:n.*79G>T
ENST00000256078.8:c.*200G>T	ENSP00000256078.4:n.*200G>T
ENST00000311936.7:c.*79G>T	ENSP00000308495.3:n.*79G>T
ENST00000557334.5:c.*79G>T	ENSP00000452512.1:n.*79G>T
NM_004985.4:c.*79G>T	NP_004976.2:n.*79G>T
NM_033360.3:c.*200G>T	NP_203524.1:n.*200G>T
XM_011520653.1:c.*79G>T	XP_011518955.1:n.*79G>T
XM_011520653.3:c.*79G>T	XP_011518955.1:n.*79G>T
NM_001369786.1:c.*200G>T	NP_001356715.1:n.*200G>T
NM_001369787.1:c.*79G>T	NP_001356716.1:n.*79G>T
NM_004985.5:c.*79G>T MANE Select	NP_004976.2:n.*79G>T
NM_033360.4:c.*200G>T MANE Plus Clinical	NP_203524.1:n.*200G>T