Canonical Allele Identifier: CA6486817

Gene: KRAS

Linked Data

• dbSNP Id: rs759430622
• ExAC: 12:25362692 G / C
• gnomAD v2: 12-25362692-G-C
• gnomAD v4: 12-25209758-G-C
• MyVariant Identifiers: chr12:g.25362692G>C (hg19) ; chr12:g.25209758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209758G>C , CM000674.2:g.25209758G>C	GRCh38
NC_000012.11:g.25362692G>C , CM000674.1:g.25362692G>C	GRCh37
NC_000012.10:g.25253959G>C	NCBI36
NG_007524.1:g.46163C>G
NG_007524.2:g.46246C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*37C>G	ENSP00000452512.1:n.*37C>G
ENST00000685328.1:c.*37C>G	ENSP00000508921.1:n.*37C>G
ENST00000686877.1:c.*575C>G	ENSP00000510431.1:n.*575C>G
ENST00000687356.1:c.*302C>G	ENSP00000510511.1:n.*302C>G
ENST00000688228.1:n.1078C>G
ENST00000688940.1:c.*37C>G	ENSP00000509238.1:n.*37C>G
ENST00000690406.1:c.407C>G
ENST00000690804.1:c.*565C>G	ENSP00000508568.1:n.*565C>G
ENST00000692768.1:c.*37C>G	ENSP00000510254.1:n.*37C>G
ENST00000693229.1:c.*37C>G	ENSP00000509223.1:n.*37C>G
ENST00000256078.10:c.*158C>G MANE Plus Clinical	ENSP00000256078.5:n.*158C>G
ENST00000311936.8:c.*37C>G MANE Select	ENSP00000308495.3:n.*37C>G
ENST00000256078.8:c.*158C>G	ENSP00000256078.4:n.*158C>G
ENST00000311936.7:c.*37C>G	ENSP00000308495.3:n.*37C>G
ENST00000557334.5:c.*37C>G	ENSP00000452512.1:n.*37C>G
NM_004985.4:c.*37C>G	NP_004976.2:n.*37C>G
NM_033360.3:c.*158C>G	NP_203524.1:n.*158C>G
XM_011520653.1:c.*37C>G	XP_011518955.1:n.*37C>G
XM_011520653.3:c.*37C>G	XP_011518955.1:n.*37C>G
NM_001369786.1:c.*158C>G	NP_001356715.1:n.*158C>G
NM_001369787.1:c.*37C>G	NP_001356716.1:n.*37C>G
NM_004985.5:c.*37C>G MANE Select	NP_004976.2:n.*37C>G
NM_033360.4:c.*158C>G MANE Plus Clinical	NP_203524.1:n.*158C>G