Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206532_25206533delinsAC , CM000674.2:g.25206532_25206533delinsAC	GRCh38
NC_000012.11:g.25359466_25359467delinsAC , CM000674.1:g.25359466_25359467delinsAC	GRCh37
NC_000012.10:g.25250733_25250734delinsAC	NCBI36
NG_007524.1:g.49388_49389delinsGT
NG_007524.2:g.49471_49472delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.3262_3263delinsGT (KRAS)	ENSP00000508921.1:n.3262_3263delinsGT
ENST00000686877.1:c.3800_3801delinsGT (KRAS)	ENSP00000510431.1:n.3800_3801delinsGT
ENST00000687356.1:c.3527_3528delinsGT (KRAS)	ENSP00000510511.1:n.3527_3528delinsGT
ENST00000690406.1:c.3632_3633delinsGT (KRAS)
ENST00000692768.1:c.3262_3263delinsGT (KRAS)	ENSP00000510254.1:n.3262_3263delinsGT
ENST00000693229.1:c.3262_3263delinsGT (KRAS)	ENSP00000509223.1:n.3262_3263delinsGT
ENST00000256078.10:c.3383_3384delinsGT (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3383_3384delinsGT
ENST00000311936.8:c.3262_3263delinsGT (KRAS) MANE Select	ENSP00000308495.3:n.3262_3263delinsGT
ENST00000553788.6:c.51+2525_51+2526delinsAC (ETFRF1)	ENSP00000451938.2:n.51+2525_51+2526delinsAC
ENST00000311936.7:c.3262_3263delinsGT (KRAS)	ENSP00000308495.3:n.3262_3263delinsGT
ENST00000553788.5:c.45+2525_45+2526delinsAC (ETFRF1)	ENSP00000451938.1:n.45+2525_45+2526delinsAC
NM_004985.4:c.3262_3263delinsGT (KRAS)	NP_004976.2:n.3262_3263delinsGT
NM_033360.3:c.3383_3384delinsGT (KRAS)	NP_203524.1:n.3383_3384delinsGT
XM_011520653.1:c.3262_3263delinsGT (KRAS)	XP_011518955.1:n.3262_3263delinsGT
XM_011520653.3:c.3262_3263delinsGT (KRAS)	XP_011518955.1:n.3262_3263delinsGT
NM_001369786.1:c.3383_3384delinsGT (KRAS)	NP_001356715.1:n.3383_3384delinsGT
NM_001369787.1:c.3262_3263delinsGT (KRAS)	NP_001356716.1:n.3262_3263delinsGT
NM_004985.5:c.3262_3263delinsGT (KRAS) MANE Select	NP_004976.2:n.3262_3263delinsGT
NM_033360.4:c.3383_3384delinsGT (KRAS) MANE Plus Clinical	NP_203524.1:n.3383_3384delinsGT

HGVS	Amino-acid Change
ENST00000685328.1:c.3262_3263delinsGT (KRAS)	ENSP00000508921.1:n.3262_3263delinsGT
ENST00000686877.1:c.3800_3801delinsGT (KRAS)	ENSP00000510431.1:n.3800_3801delinsGT
ENST00000687356.1:c.3527_3528delinsGT (KRAS)	ENSP00000510511.1:n.3527_3528delinsGT
ENST00000690406.1:c.3632_3633delinsGT (KRAS)
ENST00000692768.1:c.3262_3263delinsGT (KRAS)	ENSP00000510254.1:n.3262_3263delinsGT
ENST00000693229.1:c.3262_3263delinsGT (KRAS)	ENSP00000509223.1:n.3262_3263delinsGT
ENST00000256078.10:c.3383_3384delinsGT (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3383_3384delinsGT
ENST00000311936.8:c.3262_3263delinsGT (KRAS) MANE Select	ENSP00000308495.3:n.3262_3263delinsGT
ENST00000553788.6:c.51+2525_51+2526delinsAC (ETFRF1)	ENSP00000451938.2:n.51+2525_51+2526delinsAC
ENST00000311936.7:c.3262_3263delinsGT (KRAS)	ENSP00000308495.3:n.3262_3263delinsGT
ENST00000553788.5:c.45+2525_45+2526delinsAC (ETFRF1)	ENSP00000451938.1:n.45+2525_45+2526delinsAC
NM_004985.4:c.3262_3263delinsGT (KRAS)	NP_004976.2:n.3262_3263delinsGT
NM_033360.3:c.3383_3384delinsGT (KRAS)	NP_203524.1:n.3383_3384delinsGT
XM_011520653.1:c.3262_3263delinsGT (KRAS)	XP_011518955.1:n.3262_3263delinsGT
XM_011520653.3:c.3262_3263delinsGT (KRAS)	XP_011518955.1:n.3262_3263delinsGT
NM_001369786.1:c.3383_3384delinsGT (KRAS)	NP_001356715.1:n.3383_3384delinsGT
NM_001369787.1:c.3262_3263delinsGT (KRAS)	NP_001356716.1:n.3262_3263delinsGT
NM_004985.5:c.3262_3263delinsGT (KRAS) MANE Select	NP_004976.2:n.3262_3263delinsGT
NM_033360.4:c.3383_3384delinsGT (KRAS) MANE Plus Clinical	NP_203524.1:n.3383_3384delinsGT