Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206403_25206406delinsTCAA , CM000674.2:g.25206403_25206406delinsTCAA	GRCh38
NC_000012.11:g.25359337_25359340delinsTCAA , CM000674.1:g.25359337_25359340delinsTCAA	GRCh37
NC_000012.10:g.25250604_25250607delinsTCAA	NCBI36
NG_007524.1:g.49515_49518delinsTTGA
NG_007524.2:g.49598_49601delinsTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.3389_3392delinsTTGA (KRAS)	ENSP00000508921.1:n.3389_3392delinsTTGA
ENST00000686877.1:c.3927_3930delinsTTGA (KRAS)	ENSP00000510431.1:n.3927_3930delinsTTGA
ENST00000687356.1:c.3654_3657delinsTTGA (KRAS)	ENSP00000510511.1:n.3654_3657delinsTTGA
ENST00000690406.1:c.3759_3762delinsTTGA (KRAS)
ENST00000692768.1:c.3389_3392delinsTTGA (KRAS)	ENSP00000510254.1:n.3389_3392delinsTTGA
ENST00000693229.1:c.3389_3392delinsTTGA (KRAS)	ENSP00000509223.1:n.3389_3392delinsTTGA
ENST00000256078.10:c.3510_3513delinsTTGA (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3510_3513delinsTTGA
ENST00000311936.8:c.3389_3392delinsTTGA (KRAS) MANE Select	ENSP00000308495.3:n.3389_3392delinsTTGA
ENST00000553788.6:c.51+2396_51+2399delinsTCAA (ETFRF1)	ENSP00000451938.2:n.51+2396_51+2399delinsTCAA
ENST00000311936.7:c.3389_3392delinsTTGA (KRAS)	ENSP00000308495.3:n.3389_3392delinsTTGA
ENST00000553788.5:c.45+2396_45+2399delinsTCAA (ETFRF1)	ENSP00000451938.1:n.45+2396_45+2399delinsTCAA
NM_004985.4:c.3389_3392delinsTTGA (KRAS)	NP_004976.2:n.3389_3392delinsTTGA
NM_033360.3:c.3510_3513delinsTTGA (KRAS)	NP_203524.1:n.3510_3513delinsTTGA
XM_011520653.1:c.3389_3392delinsTTGA (KRAS)	XP_011518955.1:n.3389_3392delinsTTGA
XM_011520653.3:c.3389_3392delinsTTGA (KRAS)	XP_011518955.1:n.3389_3392delinsTTGA
NM_001369786.1:c.3510_3513delinsTTGA (KRAS)	NP_001356715.1:n.3510_3513delinsTTGA
NM_001369787.1:c.3389_3392delinsTTGA (KRAS)	NP_001356716.1:n.3389_3392delinsTTGA
NM_004985.5:c.3389_3392delinsTTGA (KRAS) MANE Select	NP_004976.2:n.3389_3392delinsTTGA
NM_033360.4:c.3510_3513delinsTTGA (KRAS) MANE Plus Clinical	NP_203524.1:n.3510_3513delinsTTGA

HGVS	Amino-acid Change
ENST00000685328.1:c.3389_3392delinsTTGA (KRAS)	ENSP00000508921.1:n.3389_3392delinsTTGA
ENST00000686877.1:c.3927_3930delinsTTGA (KRAS)	ENSP00000510431.1:n.3927_3930delinsTTGA
ENST00000687356.1:c.3654_3657delinsTTGA (KRAS)	ENSP00000510511.1:n.3654_3657delinsTTGA
ENST00000690406.1:c.3759_3762delinsTTGA (KRAS)
ENST00000692768.1:c.3389_3392delinsTTGA (KRAS)	ENSP00000510254.1:n.3389_3392delinsTTGA
ENST00000693229.1:c.3389_3392delinsTTGA (KRAS)	ENSP00000509223.1:n.3389_3392delinsTTGA
ENST00000256078.10:c.3510_3513delinsTTGA (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3510_3513delinsTTGA
ENST00000311936.8:c.3389_3392delinsTTGA (KRAS) MANE Select	ENSP00000308495.3:n.3389_3392delinsTTGA
ENST00000553788.6:c.51+2396_51+2399delinsTCAA (ETFRF1)	ENSP00000451938.2:n.51+2396_51+2399delinsTCAA
ENST00000311936.7:c.3389_3392delinsTTGA (KRAS)	ENSP00000308495.3:n.3389_3392delinsTTGA
ENST00000553788.5:c.45+2396_45+2399delinsTCAA (ETFRF1)	ENSP00000451938.1:n.45+2396_45+2399delinsTCAA
NM_004985.4:c.3389_3392delinsTTGA (KRAS)	NP_004976.2:n.3389_3392delinsTTGA
NM_033360.3:c.3510_3513delinsTTGA (KRAS)	NP_203524.1:n.3510_3513delinsTTGA
XM_011520653.1:c.3389_3392delinsTTGA (KRAS)	XP_011518955.1:n.3389_3392delinsTTGA
XM_011520653.3:c.3389_3392delinsTTGA (KRAS)	XP_011518955.1:n.3389_3392delinsTTGA
NM_001369786.1:c.3510_3513delinsTTGA (KRAS)	NP_001356715.1:n.3510_3513delinsTTGA
NM_001369787.1:c.3389_3392delinsTTGA (KRAS)	NP_001356716.1:n.3389_3392delinsTTGA
NM_004985.5:c.3389_3392delinsTTGA (KRAS) MANE Select	NP_004976.2:n.3389_3392delinsTTGA
NM_033360.4:c.3510_3513delinsTTGA (KRAS) MANE Plus Clinical	NP_203524.1:n.3510_3513delinsTTGA