Canonical Allele Identifier: CA2022898029

Gene: KRAS

Linked Data

• dbSNP Id: rs1951662727
• gnomAD v4: 12-25245238-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245239del , CM000674.2:g.25245239del	GRCh38
NC_000012.11:g.25398173del , CM000674.1:g.25398173del	GRCh37
NC_000012.10:g.25289440del	NCBI36
NG_007524.1:g.10682del
NG_007524.2:g.10765del

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.111+35del	ENSP00000451856.1:n.111+35del
ENST00000557334.6:c.111+35del	ENSP00000452512.1:n.111+35del
ENST00000685328.1:c.111+35del	ENSP00000508921.1:n.111+35del
ENST00000686877.1:c.111+35del	ENSP00000510431.1:n.111+35del
ENST00000686969.1:c.111+35del	ENSP00000510479.1:n.111+35del
ENST00000687356.1:c.111+35del	ENSP00000510511.1:n.111+35del
ENST00000688940.1:c.111+35del	ENSP00000509238.1:n.111+35del
ENST00000690804.1:c.111+35del	ENSP00000508568.1:n.111+35del
ENST00000692768.1:c.-88+5512del	ENSP00000510254.1:n.-88+5512del
ENST00000693229.1:c.111+35del	ENSP00000509223.1:n.111+35del
ENST00000256078.10:c.111+35del MANE Plus Clinical	ENSP00000256078.5:n.111+35del
ENST00000311936.8:c.111+35del MANE Select	ENSP00000308495.3:n.111+35del
ENST00000256078.8:c.111+35del	ENSP00000256078.4:n.111+35del
ENST00000311936.7:c.111+35del	ENSP00000308495.3:n.111+35del
ENST00000556131.1:c.111+35del	ENSP00000451856.1:n.111+35del
ENST00000557334.5:c.111+35del	ENSP00000452512.1:n.111+35del
NM_004985.4:c.111+35del	NP_004976.2:n.111+35del
NM_033360.3:c.111+35del	NP_203524.1:n.111+35del
XM_006719069.2:c.111+35del	XP_006719132.1:n.111+35del
XM_011520653.1:c.111+35del	XP_011518955.1:n.111+35del
XM_006719069.4:c.111+35del	XP_006719132.1:n.111+35del
XM_011520653.3:c.111+35del	XP_011518955.1:n.111+35del
NM_001369786.1:c.111+35del	NP_001356715.1:n.111+35del
NM_001369787.1:c.111+35del	NP_001356716.1:n.111+35del
NM_004985.5:c.111+35del MANE Select	NP_004976.2:n.111+35del
NM_033360.4:c.111+35del MANE Plus Clinical	NP_203524.1:n.111+35del