Canonical Allele Identifier: CA945756214

Gene: KRAS ETFRF1

Linked Data

• gnomAD v3: 12-25209617-T-TCA
• gnomAD v4: 12-25209617-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209617_25209618insCA , CM000674.2:g.25209617_25209618insCA	GRCh38
NC_000012.11:g.25362551_25362552insCA , CM000674.1:g.25362551_25362552insCA	GRCh37
NC_000012.10:g.25253818_25253819insCA	NCBI36
NG_007524.1:g.46303_46304insTG
NG_007524.2:g.46386_46387insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*177_*178insTG (KRAS)	ENSP00000452512.1:n.*177_*178insTG
ENST00000685328.1:c.*177_*178insTG (KRAS)	ENSP00000508921.1:n.*177_*178insTG
ENST00000686877.1:c.*715_*716insTG (KRAS)	ENSP00000510431.1:n.*715_*716insTG
ENST00000687356.1:c.*442_*443insTG (KRAS)	ENSP00000510511.1:n.*442_*443insTG
ENST00000688940.1:c.*177_*178insTG (KRAS)	ENSP00000509238.1:n.*177_*178insTG
ENST00000690406.1:c.547_548insTG (KRAS)
ENST00000690804.1:c.*705_*706insTG (KRAS)	ENSP00000508568.1:n.*705_*706insTG
ENST00000692768.1:c.*177_*178insTG (KRAS)	ENSP00000510254.1:n.*177_*178insTG
ENST00000693229.1:c.*177_*178insTG (KRAS)	ENSP00000509223.1:n.*177_*178insTG
ENST00000256078.10:c.*298_*299insTG (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*298_*299insTG
ENST00000311936.8:c.*177_*178insTG (KRAS) MANE Select	ENSP00000308495.3:n.*177_*178insTG
ENST00000553788.6:c.*354_*355insCA (ETFRF1)	ENSP00000451938.2:n.*354_*355insCA
ENST00000256078.8:c.*298_*299insTG (KRAS)	ENSP00000256078.4:n.*298_*299insTG
ENST00000311936.7:c.*177_*178insTG (KRAS)	ENSP00000308495.3:n.*177_*178insTG
ENST00000553788.5:c.*354_*355insCA (ETFRF1)	ENSP00000451938.1:n.*354_*355insCA
ENST00000557334.5:c.*177_*178insTG (KRAS)	ENSP00000452512.1:n.*177_*178insTG
NM_004985.4:c.*177_*178insTG (KRAS)	NP_004976.2:n.*177_*178insTG
NM_033360.3:c.*298_*299insTG (KRAS)	NP_203524.1:n.*298_*299insTG
XM_011520653.1:c.*177_*178insTG (KRAS)	XP_011518955.1:n.*177_*178insTG
XM_011520653.3:c.*177_*178insTG (KRAS)	XP_011518955.1:n.*177_*178insTG
NM_001369786.1:c.*298_*299insTG (KRAS)	NP_001356715.1:n.*298_*299insTG
NM_001369787.1:c.*177_*178insTG (KRAS)	NP_001356716.1:n.*177_*178insTG
NM_004985.5:c.*177_*178insTG (KRAS) MANE Select	NP_004976.2:n.*177_*178insTG
NM_033360.4:c.*298_*299insTG (KRAS) MANE Plus Clinical	NP_203524.1:n.*298_*299insTG