Canonical Allele Identifier: CA180646

Gene: KRAS

Linked Data

• ClinVar Variation Id: 177714
• ClinVar RCV Id: RCV000154320 ; RCV002056051 ; RCV002498737
• dbSNP Id: rs727504298
• ExAC: 12:25380355 G / A
• gnomAD v2: 12-25380355-G-A
• gnomAD v4: 12-25227421-G-A
• MyVariant Identifiers: chr12:g.25380355G>A (hg19) ; chr12:g.25227421G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227421G>A , CM000674.2:g.25227421G>A	GRCh38
NC_000012.11:g.25380355G>A , CM000674.1:g.25380355G>A	GRCh37
NC_000012.10:g.25271622G>A	NCBI36
NG_007524.1:g.28500C>T
NG_007524.2:g.28583C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17510C>T	ENSP00000452512.1:n.112-17510C>T
ENST00000685328.1:c.112-9C>T	ENSP00000508921.1:n.112-9C>T
ENST00000686877.1:c.*83-9C>T	ENSP00000510431.1:n.*83-9C>T
ENST00000687356.1:c.112-1648C>T	ENSP00000510511.1:n.112-1648C>T
ENST00000688228.1:n.577C>T
ENST00000688940.1:c.112-9C>T	ENSP00000509238.1:n.112-9C>T
ENST00000690804.1:c.*73-9C>T	ENSP00000508568.1:n.*73-9C>T
ENST00000692768.1:c.-87-9C>T	ENSP00000510254.1:n.-87-9C>T
ENST00000693229.1:c.112-84C>T	ENSP00000509223.1:n.112-84C>T
ENST00000256078.10:c.112-9C>T MANE Plus Clinical	ENSP00000256078.5:n.112-9C>T
ENST00000311936.8:c.112-9C>T MANE Select	ENSP00000308495.3:n.112-9C>T
ENST00000256078.8:c.112-9C>T	ENSP00000256078.4:n.112-9C>T
ENST00000311936.7:c.112-9C>T	ENSP00000308495.3:n.112-9C>T
ENST00000557334.5:c.112-17510C>T	ENSP00000452512.1:n.112-17510C>T
NM_004985.4:c.112-9C>T	NP_004976.2:n.112-9C>T
NM_033360.3:c.112-9C>T	NP_203524.1:n.112-9C>T
XM_006719069.2:c.112-9C>T	XP_006719132.1:n.112-9C>T
XM_011520653.1:c.112-9C>T	XP_011518955.1:n.112-9C>T
XM_006719069.4:c.112-9C>T	XP_006719132.1:n.112-9C>T
XM_011520653.3:c.112-9C>T	XP_011518955.1:n.112-9C>T
NM_001369786.1:c.112-9C>T	NP_001356715.1:n.112-9C>T
NM_001369787.1:c.112-9C>T	NP_001356716.1:n.112-9C>T
NM_004985.5:c.112-9C>T MANE Select	NP_004976.2:n.112-9C>T
NM_033360.4:c.112-9C>T MANE Plus Clinical	NP_203524.1:n.112-9C>T