Canonical Allele Identifier: CA478890008

Gene: KRAS

Linked Data

• dbSNP Id: rs1951383060
• gnomAD v4: 12-25225644-A-G
• MyVariant Identifiers: chr12:g.25378578A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225644A>G , CM000674.2:g.25225644A>G	GRCh38
NC_000012.11:g.25378578A>G , CM000674.1:g.25378578A>G	GRCh37
NC_000012.10:g.25269845A>G	NCBI36
NG_007524.1:g.30277T>C
NG_007524.2:g.30360T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15733T>C	ENSP00000452512.1:n.112-15733T>C
ENST00000685328.1:c.420T>C	ENSP00000508921.1:p.Pro140=
ENST00000686877.1:c.*391T>C	ENSP00000510431.1:n.*391T>C
ENST00000687356.1:c.*118T>C	ENSP00000510511.1:n.*118T>C
ENST00000688228.1:n.894T>C
ENST00000688940.1:c.420T>C	ENSP00000509238.1:p.Pro140=
ENST00000690406.1:c.130T>C
ENST00000690804.1:c.*381T>C	ENSP00000508568.1:n.*381T>C
ENST00000692768.1:c.222T>C	ENSP00000510254.1:p.Pro74=
ENST00000693229.1:c.345T>C	ENSP00000509223.1:p.Pro115=
ENST00000256078.10:c.420T>C MANE Plus Clinical	ENSP00000256078.5:p.Pro140=
ENST00000311936.8:c.420T>C MANE Select	ENSP00000308495.3:p.Pro140=
ENST00000256078.8:c.420T>C	ENSP00000256078.4:p.Pro140=
ENST00000311936.7:c.420T>C	ENSP00000308495.3:p.Pro140=
ENST00000557334.5:c.112-15733T>C	ENSP00000452512.1:n.112-15733T>C
NM_004985.4:c.420T>C	NP_004976.2:p.Pro140=
NM_033360.3:c.420T>C	NP_203524.1:p.Pro140=
XM_006719069.2:c.420T>C	XP_006719132.1:p.Pro140=
XM_011520653.1:c.420T>C	XP_011518955.1:p.Pro140=
XM_006719069.4:c.420T>C	XP_006719132.1:p.Pro140=
XM_011520653.3:c.420T>C	XP_011518955.1:p.Pro140=
NM_001369786.1:c.420T>C	NP_001356715.1:p.Pro140=
NM_001369787.1:c.420T>C	NP_001356716.1:p.Pro140=
NM_004985.5:c.420T>C MANE Select	NP_004976.2:p.Pro140=
NM_033360.4:c.420T>C MANE Plus Clinical	NP_203524.1:p.Pro140=