Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206265_25206266delinsCA , CM000674.2:g.25206265_25206266delinsCA	GRCh38
NC_000012.11:g.25359199_25359200delinsCA , CM000674.1:g.25359199_25359200delinsCA	GRCh37
NC_000012.10:g.25250466_25250467delinsCA	NCBI36
NG_007524.1:g.49655_49656delinsTG
NG_007524.2:g.49738_49739delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.3529_3530delinsTG (KRAS)	ENSP00000508921.1:n.3529_3530delinsTG
ENST00000686877.1:c.4067_4068delinsTG (KRAS)	ENSP00000510431.1:n.4067_4068delinsTG
ENST00000687356.1:c.3794_3795delinsTG (KRAS)	ENSP00000510511.1:n.3794_3795delinsTG
ENST00000690406.1:c.3899_3900delinsTG (KRAS)
ENST00000692768.1:c.3529_3530delinsTG (KRAS)	ENSP00000510254.1:n.3529_3530delinsTG
ENST00000693229.1:c.3529_3530delinsTG (KRAS)	ENSP00000509223.1:n.3529_3530delinsTG
ENST00000256078.10:c.3650_3651delinsTG (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3650_3651delinsTG
ENST00000311936.8:c.3529_3530delinsTG (KRAS) MANE Select	ENSP00000308495.3:n.3529_3530delinsTG
ENST00000553788.6:c.51+2258_51+2259delinsCA (ETFRF1)	ENSP00000451938.2:n.51+2258_51+2259delinsCA
ENST00000311936.7:c.3529_3530delinsTG (KRAS)	ENSP00000308495.3:n.3529_3530delinsTG
ENST00000553788.5:c.45+2258_45+2259delinsCA (ETFRF1)	ENSP00000451938.1:n.45+2258_45+2259delinsCA
NM_004985.4:c.3529_3530delinsTG (KRAS)	NP_004976.2:n.3529_3530delinsTG
NM_033360.3:c.3650_3651delinsTG (KRAS)	NP_203524.1:n.3650_3651delinsTG
XM_011520653.1:c.3529_3530delinsTG (KRAS)	XP_011518955.1:n.3529_3530delinsTG
XM_011520653.3:c.3529_3530delinsTG (KRAS)	XP_011518955.1:n.3529_3530delinsTG
NM_001369786.1:c.3650_3651delinsTG (KRAS)	NP_001356715.1:n.3650_3651delinsTG
NM_001369787.1:c.3529_3530delinsTG (KRAS)	NP_001356716.1:n.3529_3530delinsTG
NM_004985.5:c.3529_3530delinsTG (KRAS) MANE Select	NP_004976.2:n.3529_3530delinsTG
NM_033360.4:c.3650_3651delinsTG (KRAS) MANE Plus Clinical	NP_203524.1:n.3650_3651delinsTG

HGVS	Amino-acid Change
ENST00000685328.1:c.3529_3530delinsTG (KRAS)	ENSP00000508921.1:n.3529_3530delinsTG
ENST00000686877.1:c.4067_4068delinsTG (KRAS)	ENSP00000510431.1:n.4067_4068delinsTG
ENST00000687356.1:c.3794_3795delinsTG (KRAS)	ENSP00000510511.1:n.3794_3795delinsTG
ENST00000690406.1:c.3899_3900delinsTG (KRAS)
ENST00000692768.1:c.3529_3530delinsTG (KRAS)	ENSP00000510254.1:n.3529_3530delinsTG
ENST00000693229.1:c.3529_3530delinsTG (KRAS)	ENSP00000509223.1:n.3529_3530delinsTG
ENST00000256078.10:c.3650_3651delinsTG (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3650_3651delinsTG
ENST00000311936.8:c.3529_3530delinsTG (KRAS) MANE Select	ENSP00000308495.3:n.3529_3530delinsTG
ENST00000553788.6:c.51+2258_51+2259delinsCA (ETFRF1)	ENSP00000451938.2:n.51+2258_51+2259delinsCA
ENST00000311936.7:c.3529_3530delinsTG (KRAS)	ENSP00000308495.3:n.3529_3530delinsTG
ENST00000553788.5:c.45+2258_45+2259delinsCA (ETFRF1)	ENSP00000451938.1:n.45+2258_45+2259delinsCA
NM_004985.4:c.3529_3530delinsTG (KRAS)	NP_004976.2:n.3529_3530delinsTG
NM_033360.3:c.3650_3651delinsTG (KRAS)	NP_203524.1:n.3650_3651delinsTG
XM_011520653.1:c.3529_3530delinsTG (KRAS)	XP_011518955.1:n.3529_3530delinsTG
XM_011520653.3:c.3529_3530delinsTG (KRAS)	XP_011518955.1:n.3529_3530delinsTG
NM_001369786.1:c.3650_3651delinsTG (KRAS)	NP_001356715.1:n.3650_3651delinsTG
NM_001369787.1:c.3529_3530delinsTG (KRAS)	NP_001356716.1:n.3529_3530delinsTG
NM_004985.5:c.3529_3530delinsTG (KRAS) MANE Select	NP_004976.2:n.3529_3530delinsTG
NM_033360.4:c.3650_3651delinsTG (KRAS) MANE Plus Clinical	NP_203524.1:n.3650_3651delinsTG