Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208217_25208218delinsTG , CM000674.2:g.25208217_25208218delinsTG	GRCh38
NC_000012.11:g.25361151_25361152delinsTG , CM000674.1:g.25361151_25361152delinsTG	GRCh37
NC_000012.10:g.25252418_25252419delinsTG	NCBI36
NG_007524.1:g.47703_47704delinsCA
NG_007524.2:g.47786_47787delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.1577_1578delinsCA (KRAS)	ENSP00000508921.1:n.1577_1578delinsCA
ENST00000686877.1:c.2115_2116delinsCA (KRAS)	ENSP00000510431.1:n.2115_2116delinsCA
ENST00000687356.1:c.1842_1843delinsCA (KRAS)	ENSP00000510511.1:n.1842_1843delinsCA
ENST00000688940.1:c.1577_1578delinsCA (KRAS)	ENSP00000509238.1:n.1577_1578delinsCA
ENST00000690406.1:c.1947_1948delinsCA (KRAS)
ENST00000690804.1:c.2105_2106delinsCA (KRAS)	ENSP00000508568.1:n.2105_2106delinsCA
ENST00000692768.1:c.1577_1578delinsCA (KRAS)	ENSP00000510254.1:n.1577_1578delinsCA
ENST00000693229.1:c.1577_1578delinsCA (KRAS)	ENSP00000509223.1:n.1577_1578delinsCA
ENST00000256078.10:c.1698_1699delinsCA (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.1698_1699delinsCA
ENST00000311936.8:c.1577_1578delinsCA (KRAS) MANE Select	ENSP00000308495.3:n.1577_1578delinsCA
ENST00000553788.6:c.52-978_52-977delinsTG (ETFRF1)	ENSP00000451938.2:n.52-978_52-977delinsTG
ENST00000311936.7:c.1577_1578delinsCA (KRAS)	ENSP00000308495.3:n.1577_1578delinsCA
ENST00000553788.5:c.46-978_46-977delinsTG (ETFRF1)	ENSP00000451938.1:n.46-978_46-977delinsTG
NM_004985.4:c.1577_1578delinsCA (KRAS)	NP_004976.2:n.1577_1578delinsCA
NM_033360.3:c.1698_1699delinsCA (KRAS)	NP_203524.1:n.1698_1699delinsCA
XM_011520653.1:c.1577_1578delinsCA (KRAS)	XP_011518955.1:n.1577_1578delinsCA
XM_011520653.3:c.1577_1578delinsCA (KRAS)	XP_011518955.1:n.1577_1578delinsCA
NM_001369786.1:c.1698_1699delinsCA (KRAS)	NP_001356715.1:n.1698_1699delinsCA
NM_001369787.1:c.1577_1578delinsCA (KRAS)	NP_001356716.1:n.1577_1578delinsCA
NM_004985.5:c.1577_1578delinsCA (KRAS) MANE Select	NP_004976.2:n.1577_1578delinsCA
NM_033360.4:c.1698_1699delinsCA (KRAS) MANE Plus Clinical	NP_203524.1:n.1698_1699delinsCA

HGVS	Amino-acid Change
ENST00000685328.1:c.1577_1578delinsCA (KRAS)	ENSP00000508921.1:n.1577_1578delinsCA
ENST00000686877.1:c.2115_2116delinsCA (KRAS)	ENSP00000510431.1:n.2115_2116delinsCA
ENST00000687356.1:c.1842_1843delinsCA (KRAS)	ENSP00000510511.1:n.1842_1843delinsCA
ENST00000688940.1:c.1577_1578delinsCA (KRAS)	ENSP00000509238.1:n.1577_1578delinsCA
ENST00000690406.1:c.1947_1948delinsCA (KRAS)
ENST00000690804.1:c.2105_2106delinsCA (KRAS)	ENSP00000508568.1:n.2105_2106delinsCA
ENST00000692768.1:c.1577_1578delinsCA (KRAS)	ENSP00000510254.1:n.1577_1578delinsCA
ENST00000693229.1:c.1577_1578delinsCA (KRAS)	ENSP00000509223.1:n.1577_1578delinsCA
ENST00000256078.10:c.1698_1699delinsCA (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.1698_1699delinsCA
ENST00000311936.8:c.1577_1578delinsCA (KRAS) MANE Select	ENSP00000308495.3:n.1577_1578delinsCA
ENST00000553788.6:c.52-978_52-977delinsTG (ETFRF1)	ENSP00000451938.2:n.52-978_52-977delinsTG
ENST00000311936.7:c.1577_1578delinsCA (KRAS)	ENSP00000308495.3:n.1577_1578delinsCA
ENST00000553788.5:c.46-978_46-977delinsTG (ETFRF1)	ENSP00000451938.1:n.46-978_46-977delinsTG
NM_004985.4:c.1577_1578delinsCA (KRAS)	NP_004976.2:n.1577_1578delinsCA
NM_033360.3:c.1698_1699delinsCA (KRAS)	NP_203524.1:n.1698_1699delinsCA
XM_011520653.1:c.1577_1578delinsCA (KRAS)	XP_011518955.1:n.1577_1578delinsCA
XM_011520653.3:c.1577_1578delinsCA (KRAS)	XP_011518955.1:n.1577_1578delinsCA
NM_001369786.1:c.1698_1699delinsCA (KRAS)	NP_001356715.1:n.1698_1699delinsCA
NM_001369787.1:c.1577_1578delinsCA (KRAS)	NP_001356716.1:n.1577_1578delinsCA
NM_004985.5:c.1577_1578delinsCA (KRAS) MANE Select	NP_004976.2:n.1577_1578delinsCA
NM_033360.4:c.1698_1699delinsCA (KRAS) MANE Plus Clinical	NP_203524.1:n.1698_1699delinsCA