Canonical Allele Identifier: CA384151045

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378555G>T (hg19) ; chr12:g.25225621G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225621G>T , CM000674.2:g.25225621G>T	GRCh38
NC_000012.11:g.25378555G>T , CM000674.1:g.25378555G>T	GRCh37
NC_000012.10:g.25269822G>T	NCBI36
NG_007524.1:g.30300C>A
NG_007524.2:g.30383C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15710C>A	ENSP00000452512.1:n.112-15710C>A
ENST00000685328.1:c.443C>A	ENSP00000508921.1:p.Thr148Lys
ENST00000686877.1:c.*414C>A	ENSP00000510431.1:n.*414C>A
ENST00000687356.1:c.*141C>A	ENSP00000510511.1:n.*141C>A
ENST00000688228.1:n.917C>A
ENST00000688940.1:c.443C>A	ENSP00000509238.1:p.Thr148Lys
ENST00000690406.1:c.153C>A
ENST00000690804.1:c.*404C>A	ENSP00000508568.1:n.*404C>A
ENST00000692768.1:c.245C>A	ENSP00000510254.1:p.Thr82Lys
ENST00000693229.1:c.368C>A	ENSP00000509223.1:p.Thr123Lys
ENST00000256078.10:c.443C>A MANE Plus Clinical	ENSP00000256078.5:p.Thr148Lys
ENST00000311936.8:c.443C>A MANE Select	ENSP00000308495.3:p.Thr148Lys
ENST00000256078.8:c.443C>A	ENSP00000256078.4:p.Thr148Lys
ENST00000311936.7:c.443C>A	ENSP00000308495.3:p.Thr148Lys
ENST00000557334.5:c.112-15710C>A	ENSP00000452512.1:n.112-15710C>A
NM_004985.4:c.443C>A	NP_004976.2:p.Thr148Lys
NM_033360.3:c.443C>A	NP_203524.1:p.Thr148Lys
XM_006719069.2:c.443C>A	XP_006719132.1:p.Thr148Lys
XM_011520653.1:c.443C>A	XP_011518955.1:p.Thr148Lys
XM_006719069.4:c.443C>A	XP_006719132.1:p.Thr148Lys
XM_011520653.3:c.443C>A	XP_011518955.1:p.Thr148Lys
NM_001369786.1:c.443C>A	NP_001356715.1:p.Thr148Lys
NM_001369787.1:c.443C>A	NP_001356716.1:p.Thr148Lys
NM_004985.5:c.443C>A MANE Select	NP_004976.2:p.Thr148Lys
NM_033360.4:c.443C>A MANE Plus Clinical	NP_203524.1:p.Thr148Lys