Canonical Allele Identifier: CA384151391

Gene: KRAS

Linked Data

• dbSNP Id: rs2141506126
• MyVariant Identifiers: chr12:g.25378633G>A (hg19) ; chr12:g.25225699G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225699G>A , CM000674.2:g.25225699G>A	GRCh38
NC_000012.11:g.25378633G>A , CM000674.1:g.25378633G>A	GRCh37
NC_000012.10:g.25269900G>A	NCBI36
NG_007524.1:g.30222C>T
NG_007524.2:g.30305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15788C>T	ENSP00000452512.1:n.112-15788C>T
ENST00000685328.1:c.365C>T	ENSP00000508921.1:p.Ser122Phe
ENST00000686877.1:c.*336C>T	ENSP00000510431.1:n.*336C>T
ENST00000687356.1:c.*63C>T	ENSP00000510511.1:n.*63C>T
ENST00000688228.1:n.839C>T
ENST00000688940.1:c.365C>T	ENSP00000509238.1:p.Ser122Phe
ENST00000690406.1:c.75C>T
ENST00000690804.1:c.*326C>T	ENSP00000508568.1:n.*326C>T
ENST00000692768.1:c.167C>T	ENSP00000510254.1:p.Ser56Phe
ENST00000693229.1:c.290C>T	ENSP00000509223.1:p.Ser97Phe
ENST00000256078.10:c.365C>T MANE Plus Clinical	ENSP00000256078.5:p.Ser122Phe
ENST00000311936.8:c.365C>T MANE Select	ENSP00000308495.3:p.Ser122Phe
ENST00000256078.8:c.365C>T	ENSP00000256078.4:p.Ser122Phe
ENST00000311936.7:c.365C>T	ENSP00000308495.3:p.Ser122Phe
ENST00000557334.5:c.112-15788C>T	ENSP00000452512.1:n.112-15788C>T
NM_004985.4:c.365C>T	NP_004976.2:p.Ser122Phe
NM_033360.3:c.365C>T	NP_203524.1:p.Ser122Phe
XM_006719069.2:c.365C>T	XP_006719132.1:p.Ser122Phe
XM_011520653.1:c.365C>T	XP_011518955.1:p.Ser122Phe
XM_006719069.4:c.365C>T	XP_006719132.1:p.Ser122Phe
XM_011520653.3:c.365C>T	XP_011518955.1:p.Ser122Phe
NM_001369786.1:c.365C>T	NP_001356715.1:p.Ser122Phe
NM_001369787.1:c.365C>T	NP_001356716.1:p.Ser122Phe
NM_004985.5:c.365C>T MANE Select	NP_004976.2:p.Ser122Phe
NM_033360.4:c.365C>T MANE Plus Clinical	NP_203524.1:p.Ser122Phe