Canonical Allele Identifier: CA234221198

Gene: KRAS

Linked Data

• ClinVar Variation Id: 2454057
• ClinVar RCV Id: RCV003188192
• dbSNP Id: rs958790148
• gnomAD v4: 12-25227356-G-A
• MyVariant Identifiers: chr12:g.25380290G>A (hg19) ; chr12:g.25227356G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227356G>A , CM000674.2:g.25227356G>A	GRCh38
NC_000012.11:g.25380290G>A , CM000674.1:g.25380290G>A	GRCh37
NC_000012.10:g.25271557G>A	NCBI36
NG_007524.1:g.28565C>T
NG_007524.2:g.28648C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17445C>T	ENSP00000452512.1:n.112-17445C>T
ENST00000685328.1:c.168C>T	ENSP00000508921.1:p.Leu56=
ENST00000686877.1:c.*139C>T	ENSP00000510431.1:n.*139C>T
ENST00000687356.1:c.112-1583C>T	ENSP00000510511.1:n.112-1583C>T
ENST00000688228.1:n.642C>T
ENST00000688940.1:c.168C>T	ENSP00000509238.1:p.Leu56=
ENST00000690804.1:c.*129C>T	ENSP00000508568.1:n.*129C>T
ENST00000692768.1:c.-31C>T	ENSP00000510254.1:n.-31C>T
ENST00000693229.1:c.112-19C>T	ENSP00000509223.1:n.112-19C>T
ENST00000256078.10:c.168C>T MANE Plus Clinical	ENSP00000256078.5:p.Leu56=
ENST00000311936.8:c.168C>T MANE Select	ENSP00000308495.3:p.Leu56=
ENST00000256078.8:c.168C>T	ENSP00000256078.4:p.Leu56=
ENST00000311936.7:c.168C>T	ENSP00000308495.3:p.Leu56=
ENST00000557334.5:c.112-17445C>T	ENSP00000452512.1:n.112-17445C>T
NM_004985.4:c.168C>T	NP_004976.2:p.Leu56=
NM_033360.3:c.168C>T	NP_203524.1:p.Leu56=
XM_006719069.2:c.168C>T	XP_006719132.1:p.Leu56=
XM_011520653.1:c.168C>T	XP_011518955.1:p.Leu56=
XM_006719069.4:c.168C>T	XP_006719132.1:p.Leu56=
XM_011520653.3:c.168C>T	XP_011518955.1:p.Leu56=
NM_001369786.1:c.168C>T	NP_001356715.1:p.Leu56=
NM_001369787.1:c.168C>T	NP_001356716.1:p.Leu56=
NM_004985.5:c.168C>T MANE Select	NP_004976.2:p.Leu56=
NM_033360.4:c.168C>T MANE Plus Clinical	NP_203524.1:p.Leu56=