Canonical Allele Identifier: CA686715052

Gene: KRAS

Linked Data

• dbSNP Id: rs1377333389
• gnomAD v3: 12-25210134-A-G
• gnomAD v4: 12-25210134-A-G
• MyVariant Identifiers: chr12:g.25363068A>G (hg19) ; chr12:g.25210134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25210134A>G , CM000674.2:g.25210134A>G	GRCh38
NC_000012.11:g.25363068A>G , CM000674.1:g.25363068A>G	GRCh37
NC_000012.10:g.25254335A>G	NCBI36
NG_007524.1:g.45787T>C
NG_007524.2:g.45870T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-223T>C	ENSP00000452512.1:n.112-223T>C
ENST00000685328.1:c.451-223T>C	ENSP00000508921.1:n.451-223T>C
ENST00000686877.1:c.*422-223T>C	ENSP00000510431.1:n.*422-223T>C
ENST00000687356.1:c.*149-223T>C	ENSP00000510511.1:n.*149-223T>C
ENST00000688228.1:n.925-223T>C
ENST00000688940.1:c.451-223T>C	ENSP00000509238.1:n.451-223T>C
ENST00000690406.1:c.254-223T>C
ENST00000690804.1:c.*412-223T>C	ENSP00000508568.1:n.*412-223T>C
ENST00000692768.1:c.253-223T>C	ENSP00000510254.1:n.253-223T>C
ENST00000693229.1:c.376-223T>C	ENSP00000509223.1:n.376-223T>C
ENST00000256078.10:c.*5-223T>C MANE Plus Clinical	ENSP00000256078.5:n.*5-223T>C
ENST00000311936.8:c.451-223T>C MANE Select	ENSP00000308495.3:n.451-223T>C
ENST00000256078.8:c.*5-223T>C	ENSP00000256078.4:n.*5-223T>C
ENST00000311936.7:c.451-223T>C	ENSP00000308495.3:n.451-223T>C
ENST00000557334.5:c.112-223T>C	ENSP00000452512.1:n.112-223T>C
NM_004985.4:c.451-223T>C	NP_004976.2:n.451-223T>C
NM_033360.3:c.*5-223T>C	NP_203524.1:n.*5-223T>C
XM_006719069.2:c.*5-223T>C	XP_006719132.1:n.*5-223T>C
XM_011520653.1:c.451-223T>C	XP_011518955.1:n.451-223T>C
XM_006719069.4:c.*5-223T>C	XP_006719132.1:n.*5-223T>C
XM_011520653.3:c.451-223T>C	XP_011518955.1:n.451-223T>C
NM_001369786.1:c.*5-223T>C	NP_001356715.1:n.*5-223T>C
NM_001369787.1:c.451-223T>C	NP_001356716.1:n.451-223T>C
NM_004985.5:c.451-223T>C MANE Select	NP_004976.2:n.451-223T>C
NM_033360.4:c.*5-223T>C MANE Plus Clinical	NP_203524.1:n.*5-223T>C