Canonical Allele Identifier: CA234219531

Gene: KRAS

Linked Data

• dbSNP Id: rs984982309
• gnomAD v3: 12-25225554-A-G
• gnomAD v4: 12-25225554-A-G
• MyVariant Identifiers: chr12:g.25378488A>G (hg19) ; chr12:g.25225554A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225554A>G , CM000674.2:g.25225554A>G	GRCh38
NC_000012.11:g.25378488A>G , CM000674.1:g.25378488A>G	GRCh37
NC_000012.10:g.25269755A>G	NCBI36
NG_007524.1:g.30367T>C
NG_007524.2:g.30450T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15643T>C	ENSP00000452512.1:n.112-15643T>C
ENST00000685328.1:c.450+60T>C	ENSP00000508921.1:n.450+60T>C
ENST00000686877.1:c.*421+60T>C	ENSP00000510431.1:n.*421+60T>C
ENST00000687356.1:c.*148+60T>C	ENSP00000510511.1:n.*148+60T>C
ENST00000688228.1:n.924+60T>C
ENST00000688940.1:c.450+60T>C	ENSP00000509238.1:n.450+60T>C
ENST00000690406.1:c.160+60T>C
ENST00000690804.1:c.*411+60T>C	ENSP00000508568.1:n.*411+60T>C
ENST00000692768.1:c.252+60T>C	ENSP00000510254.1:n.252+60T>C
ENST00000693229.1:c.375+60T>C	ENSP00000509223.1:n.375+60T>C
ENST00000256078.10:c.450+60T>C MANE Plus Clinical	ENSP00000256078.5:n.450+60T>C
ENST00000311936.8:c.450+60T>C MANE Select	ENSP00000308495.3:n.450+60T>C
ENST00000256078.8:c.450+60T>C	ENSP00000256078.4:n.450+60T>C
ENST00000311936.7:c.450+60T>C	ENSP00000308495.3:n.450+60T>C
ENST00000557334.5:c.112-15643T>C	ENSP00000452512.1:n.112-15643T>C
NM_004985.4:c.450+60T>C	NP_004976.2:n.450+60T>C
NM_033360.3:c.450+60T>C	NP_203524.1:n.450+60T>C
XM_006719069.2:c.450+60T>C	XP_006719132.1:n.450+60T>C
XM_011520653.1:c.450+60T>C	XP_011518955.1:n.450+60T>C
XM_006719069.4:c.450+60T>C	XP_006719132.1:n.450+60T>C
XM_011520653.3:c.450+60T>C	XP_011518955.1:n.450+60T>C
NM_001369786.1:c.450+60T>C	NP_001356715.1:n.450+60T>C
NM_001369787.1:c.450+60T>C	NP_001356716.1:n.450+60T>C
NM_004985.5:c.450+60T>C MANE Select	NP_004976.2:n.450+60T>C
NM_033360.4:c.450+60T>C MANE Plus Clinical	NP_203524.1:n.450+60T>C