Canonical Allele Identifier: CA384149138

Gene: KRAS

Linked Data

• dbSNP Id: rs4362222
• MyVariant Identifiers: chr12:g.25215528T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215528T>A , CM000674.2:g.25215528T>A	GRCh38
NG_007524.2:g.40476A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5617A>T	ENSP00000452512.1:n.112-5617A>T
ENST00000685328.1:c.451-5617A>T	ENSP00000508921.1:n.451-5617A>T
ENST00000686877.1:c.*422-5617A>T	ENSP00000510431.1:n.*422-5617A>T
ENST00000687356.1:c.*149-5617A>T	ENSP00000510511.1:n.*149-5617A>T
ENST00000688228.1:n.925-5617A>T
ENST00000688940.1:c.451-5617A>T	ENSP00000509238.1:n.451-5617A>T
ENST00000690406.1:c.161-2322A>T
ENST00000690804.1:c.*412-5617A>T	ENSP00000508568.1:n.*412-5617A>T
ENST00000692768.1:c.253-5617A>T	ENSP00000510254.1:n.253-5617A>T
ENST00000693229.1:c.376-5617A>T	ENSP00000509223.1:n.376-5617A>T
ENST00000256078.10:c.483A>T MANE Plus Clinical	ENSP00000256078.5:p.Arg161Ser
ENST00000311936.8:c.451-5617A>T MANE Select	ENSP00000308495.3:n.451-5617A>T
ENST00000256078.8:c.483A>T	ENSP00000256078.4:p.Arg161Ser
ENST00000311936.7:c.451-5617A>T	ENSP00000308495.3:n.451-5617A>T
ENST00000557334.5:c.112-5617A>T	ENSP00000452512.1:n.112-5617A>T
NM_004985.4:c.451-5617A>T	NP_004976.2:n.451-5617A>T
XM_006719069.2:c.483A>T	XP_006719132.1:p.Arg161Ser
XM_011520653.1:c.451-5617A>T	XP_011518955.1:n.451-5617A>T
XM_006719069.4:c.483A>T	XP_006719132.1:p.Arg161Ser
XM_011520653.3:c.451-5617A>T	XP_011518955.1:n.451-5617A>T
NM_001369786.1:c.483A>T	NP_001356715.1:p.Arg161Ser
NM_001369787.1:c.451-5617A>T	NP_001356716.1:n.451-5617A>T
NM_004985.5:c.451-5617A>T MANE Select	NP_004976.2:n.451-5617A>T
NM_033360.4:c.483A>T MANE Plus Clinical	NP_203524.1:p.Arg161Ser