Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208066_25208067insAT , CM000674.2:g.25208066_25208067insAT	GRCh38
NC_000012.11:g.25361000_25361001insAT , CM000674.1:g.25361000_25361001insAT	GRCh37
NC_000012.10:g.25252267_25252268insAT	NCBI36
NG_007524.1:g.47854_47855insAT
NG_007524.2:g.47937_47938insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.1728_1729insAT (KRAS)	ENSP00000508921.1:n.1728_1729insAT
ENST00000686877.1:c.2266_2267insAT (KRAS)	ENSP00000510431.1:n.2266_2267insAT
ENST00000687356.1:c.1993_1994insAT (KRAS)	ENSP00000510511.1:n.1993_1994insAT
ENST00000688940.1:c.1728_1729insAT (KRAS)	ENSP00000509238.1:n.1728_1729insAT
ENST00000690406.1:c.2098_2099insAT (KRAS)
ENST00000690804.1:c.2256_2257insAT (KRAS)	ENSP00000508568.1:n.2256_2257insAT
ENST00000692768.1:c.1728_1729insAT (KRAS)	ENSP00000510254.1:n.1728_1729insAT
ENST00000693229.1:c.1728_1729insAT (KRAS)	ENSP00000509223.1:n.1728_1729insAT
ENST00000256078.10:c.1849_1850insAT (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.1849_1850insAT
ENST00000311936.8:c.1728_1729insAT (KRAS) MANE Select	ENSP00000308495.3:n.1728_1729insAT
ENST00000553788.6:c.52-1129_52-1128insAT (ETFRF1)	ENSP00000451938.2:n.52-1129_52-1128insAT
ENST00000311936.7:c.1728_1729insAT (KRAS)	ENSP00000308495.3:n.1728_1729insAT
ENST00000553788.5:c.46-1129_46-1128insAT (ETFRF1)	ENSP00000451938.1:n.46-1129_46-1128insAT
NM_004985.4:c.1728_1729insAT (KRAS)	NP_004976.2:n.1728_1729insAT
NM_033360.3:c.1849_1850insAT (KRAS)	NP_203524.1:n.1849_1850insAT
XM_011520653.1:c.1728_1729insAT (KRAS)	XP_011518955.1:n.1728_1729insAT
XM_011520653.3:c.1728_1729insAT (KRAS)	XP_011518955.1:n.1728_1729insAT
NM_001369786.1:c.1849_1850insAT (KRAS)	NP_001356715.1:n.1849_1850insAT
NM_001369787.1:c.1728_1729insAT (KRAS)	NP_001356716.1:n.1728_1729insAT
NM_004985.5:c.1728_1729insAT (KRAS) MANE Select	NP_004976.2:n.1728_1729insAT
NM_033360.4:c.1849_1850insAT (KRAS) MANE Plus Clinical	NP_203524.1:n.1849_1850insAT

HGVS	Amino-acid Change
ENST00000685328.1:c.1728_1729insAT (KRAS)	ENSP00000508921.1:n.1728_1729insAT
ENST00000686877.1:c.2266_2267insAT (KRAS)	ENSP00000510431.1:n.2266_2267insAT
ENST00000687356.1:c.1993_1994insAT (KRAS)	ENSP00000510511.1:n.1993_1994insAT
ENST00000688940.1:c.1728_1729insAT (KRAS)	ENSP00000509238.1:n.1728_1729insAT
ENST00000690406.1:c.2098_2099insAT (KRAS)
ENST00000690804.1:c.2256_2257insAT (KRAS)	ENSP00000508568.1:n.2256_2257insAT
ENST00000692768.1:c.1728_1729insAT (KRAS)	ENSP00000510254.1:n.1728_1729insAT
ENST00000693229.1:c.1728_1729insAT (KRAS)	ENSP00000509223.1:n.1728_1729insAT
ENST00000256078.10:c.1849_1850insAT (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.1849_1850insAT
ENST00000311936.8:c.1728_1729insAT (KRAS) MANE Select	ENSP00000308495.3:n.1728_1729insAT
ENST00000553788.6:c.52-1129_52-1128insAT (ETFRF1)	ENSP00000451938.2:n.52-1129_52-1128insAT
ENST00000311936.7:c.1728_1729insAT (KRAS)	ENSP00000308495.3:n.1728_1729insAT
ENST00000553788.5:c.46-1129_46-1128insAT (ETFRF1)	ENSP00000451938.1:n.46-1129_46-1128insAT
NM_004985.4:c.1728_1729insAT (KRAS)	NP_004976.2:n.1728_1729insAT
NM_033360.3:c.1849_1850insAT (KRAS)	NP_203524.1:n.1849_1850insAT
XM_011520653.1:c.1728_1729insAT (KRAS)	XP_011518955.1:n.1728_1729insAT
XM_011520653.3:c.1728_1729insAT (KRAS)	XP_011518955.1:n.1728_1729insAT
NM_001369786.1:c.1849_1850insAT (KRAS)	NP_001356715.1:n.1849_1850insAT
NM_001369787.1:c.1728_1729insAT (KRAS)	NP_001356716.1:n.1728_1729insAT
NM_004985.5:c.1728_1729insAT (KRAS) MANE Select	NP_004976.2:n.1728_1729insAT
NM_033360.4:c.1849_1850insAT (KRAS) MANE Plus Clinical	NP_203524.1:n.1849_1850insAT