Canonical Allele Identifier: CA2617994262

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209703-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209703G>T , CM000674.2:g.25209703G>T	GRCh38
NC_000012.11:g.25362637G>T , CM000674.1:g.25362637G>T	GRCh37
NC_000012.10:g.25253904G>T	NCBI36
NG_007524.1:g.46218C>A
NG_007524.2:g.46301C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*92C>A	ENSP00000452512.1:n.*92C>A
ENST00000685328.1:c.*92C>A	ENSP00000508921.1:n.*92C>A
ENST00000686877.1:c.*630C>A	ENSP00000510431.1:n.*630C>A
ENST00000687356.1:c.*357C>A	ENSP00000510511.1:n.*357C>A
ENST00000688228.1:n.1133C>A
ENST00000688940.1:c.*92C>A	ENSP00000509238.1:n.*92C>A
ENST00000690406.1:c.462C>A
ENST00000690804.1:c.*620C>A	ENSP00000508568.1:n.*620C>A
ENST00000692768.1:c.*92C>A	ENSP00000510254.1:n.*92C>A
ENST00000693229.1:c.*92C>A	ENSP00000509223.1:n.*92C>A
ENST00000256078.10:c.*213C>A MANE Plus Clinical	ENSP00000256078.5:n.*213C>A
ENST00000311936.8:c.*92C>A MANE Select	ENSP00000308495.3:n.*92C>A
ENST00000256078.8:c.*213C>A	ENSP00000256078.4:n.*213C>A
ENST00000311936.7:c.*92C>A	ENSP00000308495.3:n.*92C>A
ENST00000557334.5:c.*92C>A	ENSP00000452512.1:n.*92C>A
NM_004985.4:c.*92C>A	NP_004976.2:n.*92C>A
NM_033360.3:c.*213C>A	NP_203524.1:n.*213C>A
XM_011520653.1:c.*92C>A	XP_011518955.1:n.*92C>A
XM_011520653.3:c.*92C>A	XP_011518955.1:n.*92C>A
NM_001369786.1:c.*213C>A	NP_001356715.1:n.*213C>A
NM_001369787.1:c.*92C>A	NP_001356716.1:n.*92C>A
NM_004985.5:c.*92C>A MANE Select	NP_004976.2:n.*92C>A
NM_033360.4:c.*213C>A MANE Plus Clinical	NP_203524.1:n.*213C>A