Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206444_25206445delinsAC , CM000674.2:g.25206444_25206445delinsAC	GRCh38
NC_000012.11:g.25359378_25359379delinsAC , CM000674.1:g.25359378_25359379delinsAC	GRCh37
NC_000012.10:g.25250645_25250646delinsAC	NCBI36
NG_007524.1:g.49476_49477delinsGT
NG_007524.2:g.49559_49560delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.3350_3351delinsGT (KRAS)	ENSP00000508921.1:n.3350_3351delinsGT
ENST00000686877.1:c.3888_3889delinsGT (KRAS)	ENSP00000510431.1:n.3888_3889delinsGT
ENST00000687356.1:c.3615_3616delinsGT (KRAS)	ENSP00000510511.1:n.3615_3616delinsGT
ENST00000690406.1:c.3720_3721delinsGT (KRAS)
ENST00000692768.1:c.3350_3351delinsGT (KRAS)	ENSP00000510254.1:n.3350_3351delinsGT
ENST00000693229.1:c.3350_3351delinsGT (KRAS)	ENSP00000509223.1:n.3350_3351delinsGT
ENST00000256078.10:c.3471_3472delinsGT (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3471_3472delinsGT
ENST00000311936.8:c.3350_3351delinsGT (KRAS) MANE Select	ENSP00000308495.3:n.3350_3351delinsGT
ENST00000553788.6:c.51+2437_51+2438delinsAC (ETFRF1)	ENSP00000451938.2:n.51+2437_51+2438delinsAC
ENST00000311936.7:c.3350_3351delinsGT (KRAS)	ENSP00000308495.3:n.3350_3351delinsGT
ENST00000553788.5:c.45+2437_45+2438delinsAC (ETFRF1)	ENSP00000451938.1:n.45+2437_45+2438delinsAC
NM_004985.4:c.3350_3351delinsGT (KRAS)	NP_004976.2:n.3350_3351delinsGT
NM_033360.3:c.3471_3472delinsGT (KRAS)	NP_203524.1:n.3471_3472delinsGT
XM_011520653.1:c.3350_3351delinsGT (KRAS)	XP_011518955.1:n.3350_3351delinsGT
XM_011520653.3:c.3350_3351delinsGT (KRAS)	XP_011518955.1:n.3350_3351delinsGT
NM_001369786.1:c.3471_3472delinsGT (KRAS)	NP_001356715.1:n.3471_3472delinsGT
NM_001369787.1:c.3350_3351delinsGT (KRAS)	NP_001356716.1:n.3350_3351delinsGT
NM_004985.5:c.3350_3351delinsGT (KRAS) MANE Select	NP_004976.2:n.3350_3351delinsGT
NM_033360.4:c.3471_3472delinsGT (KRAS) MANE Plus Clinical	NP_203524.1:n.3471_3472delinsGT

HGVS	Amino-acid Change
ENST00000685328.1:c.3350_3351delinsGT (KRAS)	ENSP00000508921.1:n.3350_3351delinsGT
ENST00000686877.1:c.3888_3889delinsGT (KRAS)	ENSP00000510431.1:n.3888_3889delinsGT
ENST00000687356.1:c.3615_3616delinsGT (KRAS)	ENSP00000510511.1:n.3615_3616delinsGT
ENST00000690406.1:c.3720_3721delinsGT (KRAS)
ENST00000692768.1:c.3350_3351delinsGT (KRAS)	ENSP00000510254.1:n.3350_3351delinsGT
ENST00000693229.1:c.3350_3351delinsGT (KRAS)	ENSP00000509223.1:n.3350_3351delinsGT
ENST00000256078.10:c.3471_3472delinsGT (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.3471_3472delinsGT
ENST00000311936.8:c.3350_3351delinsGT (KRAS) MANE Select	ENSP00000308495.3:n.3350_3351delinsGT
ENST00000553788.6:c.51+2437_51+2438delinsAC (ETFRF1)	ENSP00000451938.2:n.51+2437_51+2438delinsAC
ENST00000311936.7:c.3350_3351delinsGT (KRAS)	ENSP00000308495.3:n.3350_3351delinsGT
ENST00000553788.5:c.45+2437_45+2438delinsAC (ETFRF1)	ENSP00000451938.1:n.45+2437_45+2438delinsAC
NM_004985.4:c.3350_3351delinsGT (KRAS)	NP_004976.2:n.3350_3351delinsGT
NM_033360.3:c.3471_3472delinsGT (KRAS)	NP_203524.1:n.3471_3472delinsGT
XM_011520653.1:c.3350_3351delinsGT (KRAS)	XP_011518955.1:n.3350_3351delinsGT
XM_011520653.3:c.3350_3351delinsGT (KRAS)	XP_011518955.1:n.3350_3351delinsGT
NM_001369786.1:c.3471_3472delinsGT (KRAS)	NP_001356715.1:n.3471_3472delinsGT
NM_001369787.1:c.3350_3351delinsGT (KRAS)	NP_001356716.1:n.3350_3351delinsGT
NM_004985.5:c.3350_3351delinsGT (KRAS) MANE Select	NP_004976.2:n.3350_3351delinsGT
NM_033360.4:c.3471_3472delinsGT (KRAS) MANE Plus Clinical	NP_203524.1:n.3471_3472delinsGT