Canonical Allele Identifier: CA384148272

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362729T>A (hg19) ; chr12:g.25209795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209795T>A , CM000674.2:g.25209795T>A	GRCh38
NC_000012.11:g.25362729T>A , CM000674.1:g.25362729T>A	GRCh37
NC_000012.10:g.25253996T>A	NCBI36
NG_007524.1:g.46126A>T
NG_007524.2:g.46209A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.228A>T	ENSP00000452512.1:p.Ter76Tyr
ENST00000685328.1:c.567A>T	ENSP00000508921.1:p.Ter189Tyr
ENST00000686877.1:c.*538A>T	ENSP00000510431.1:n.*538A>T
ENST00000687356.1:c.*265A>T	ENSP00000510511.1:n.*265A>T
ENST00000688228.1:n.1041A>T
ENST00000688940.1:c.567A>T	ENSP00000509238.1:p.Ter189Tyr
ENST00000690406.1:c.370A>T
ENST00000690804.1:c.*528A>T	ENSP00000508568.1:n.*528A>T
ENST00000692768.1:c.369A>T	ENSP00000510254.1:p.Ter123Tyr
ENST00000693229.1:c.492A>T	ENSP00000509223.1:p.Ter164Tyr
ENST00000256078.10:c.*121A>T MANE Plus Clinical	ENSP00000256078.5:n.*121A>T
ENST00000311936.8:c.567A>T MANE Select	ENSP00000308495.3:p.Ter189Tyr
ENST00000256078.8:c.*121A>T	ENSP00000256078.4:n.*121A>T
ENST00000311936.7:c.567A>T	ENSP00000308495.3:p.Ter189Tyr
ENST00000557334.5:c.228A>T	ENSP00000452512.1:p.Ter76Tyr
NM_004985.4:c.567A>T	NP_004976.2:p.Ter189Tyr
NM_033360.3:c.*121A>T	NP_203524.1:n.*121A>T
XM_011520653.1:c.567A>T	XP_011518955.1:p.Ter189Tyr
XM_011520653.3:c.567A>T	XP_011518955.1:p.Ter189Tyr
NM_001369786.1:c.*121A>T	NP_001356715.1:n.*121A>T
NM_001369787.1:c.567A>T	NP_001356716.1:p.Ter189Tyr
NM_004985.5:c.567A>T MANE Select	NP_004976.2:p.Ter189Tyr
NM_033360.4:c.*121A>T MANE Plus Clinical	NP_203524.1:n.*121A>T