Canonical Allele Identifier: CA6486822

Gene: KRAS

Linked Data

• dbSNP Id: rs762532538
• ExAC: 12:25362756 C / G
• gnomAD v2: 12-25362756-C-G
• gnomAD v4: 12-25209822-C-G
• MyVariant Identifiers: chr12:g.25362756C>G (hg19) ; chr12:g.25209822C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209822C>G , CM000674.2:g.25209822C>G	GRCh38
NC_000012.11:g.25362756C>G , CM000674.1:g.25362756C>G	GRCh37
NC_000012.10:g.25254023C>G	NCBI36
NG_007524.1:g.46099G>C
NG_007524.2:g.46182G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.201G>C	ENSP00000452512.1:p.Lys67Asn
ENST00000685328.1:c.540G>C	ENSP00000508921.1:p.Lys180Asn
ENST00000686877.1:c.*511G>C	ENSP00000510431.1:n.*511G>C
ENST00000687356.1:c.*238G>C	ENSP00000510511.1:n.*238G>C
ENST00000688228.1:n.1014G>C
ENST00000688940.1:c.540G>C	ENSP00000509238.1:p.Lys180Asn
ENST00000690406.1:c.343G>C
ENST00000690804.1:c.*501G>C	ENSP00000508568.1:n.*501G>C
ENST00000692768.1:c.342G>C	ENSP00000510254.1:p.Lys114Asn
ENST00000693229.1:c.465G>C	ENSP00000509223.1:p.Lys155Asn
ENST00000256078.10:c.*94G>C MANE Plus Clinical	ENSP00000256078.5:n.*94G>C
ENST00000311936.8:c.540G>C MANE Select	ENSP00000308495.3:p.Lys180Asn
ENST00000256078.8:c.*94G>C	ENSP00000256078.4:n.*94G>C
ENST00000311936.7:c.540G>C	ENSP00000308495.3:p.Lys180Asn
ENST00000557334.5:c.201G>C	ENSP00000452512.1:p.Lys67Asn
NM_004985.4:c.540G>C	NP_004976.2:p.Lys180Asn
NM_033360.3:c.*94G>C	NP_203524.1:n.*94G>C
XM_011520653.1:c.540G>C	XP_011518955.1:p.Lys180Asn
XM_011520653.3:c.540G>C	XP_011518955.1:p.Lys180Asn
NM_001369786.1:c.*94G>C	NP_001356715.1:n.*94G>C
NM_001369787.1:c.540G>C	NP_001356716.1:p.Lys180Asn
NM_004985.5:c.540G>C MANE Select	NP_004976.2:p.Lys180Asn
NM_033360.4:c.*94G>C MANE Plus Clinical	NP_203524.1:n.*94G>C