Canonical Allele Identifier: CA384151169

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378583T>A (hg19) ; chr12:g.25225649T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225649T>A , CM000674.2:g.25225649T>A	GRCh38
NC_000012.11:g.25378583T>A , CM000674.1:g.25378583T>A	GRCh37
NC_000012.10:g.25269850T>A	NCBI36
NG_007524.1:g.30272A>T
NG_007524.2:g.30355A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15738A>T	ENSP00000452512.1:n.112-15738A>T
ENST00000685328.1:c.415A>T	ENSP00000508921.1:p.Ile139Phe
ENST00000686877.1:c.*386A>T	ENSP00000510431.1:n.*386A>T
ENST00000687356.1:c.*113A>T	ENSP00000510511.1:n.*113A>T
ENST00000688228.1:n.889A>T
ENST00000688940.1:c.415A>T	ENSP00000509238.1:p.Ile139Phe
ENST00000690406.1:c.125A>T
ENST00000690804.1:c.*376A>T	ENSP00000508568.1:n.*376A>T
ENST00000692768.1:c.217A>T	ENSP00000510254.1:p.Ile73Phe
ENST00000693229.1:c.340A>T	ENSP00000509223.1:p.Ile114Phe
ENST00000256078.10:c.415A>T MANE Plus Clinical	ENSP00000256078.5:p.Ile139Phe
ENST00000311936.8:c.415A>T MANE Select	ENSP00000308495.3:p.Ile139Phe
ENST00000256078.8:c.415A>T	ENSP00000256078.4:p.Ile139Phe
ENST00000311936.7:c.415A>T	ENSP00000308495.3:p.Ile139Phe
ENST00000557334.5:c.112-15738A>T	ENSP00000452512.1:n.112-15738A>T
NM_004985.4:c.415A>T	NP_004976.2:p.Ile139Phe
NM_033360.3:c.415A>T	NP_203524.1:p.Ile139Phe
XM_006719069.2:c.415A>T	XP_006719132.1:p.Ile139Phe
XM_011520653.1:c.415A>T	XP_011518955.1:p.Ile139Phe
XM_006719069.4:c.415A>T	XP_006719132.1:p.Ile139Phe
XM_011520653.3:c.415A>T	XP_011518955.1:p.Ile139Phe
NM_001369786.1:c.415A>T	NP_001356715.1:p.Ile139Phe
NM_001369787.1:c.415A>T	NP_001356716.1:p.Ile139Phe
NM_004985.5:c.415A>T MANE Select	NP_004976.2:p.Ile139Phe
NM_033360.4:c.415A>T MANE Plus Clinical	NP_203524.1:p.Ile139Phe