Canonical Allele Identifier: CA234206765

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs917782865
• gnomAD v3: 12-25209622-GA-G
• gnomAD v4: 12-25209622-GA-G
• MyVariant Identifiers: chr12:g.25362557del (hg19) ; chr12:g.25209623del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209631del , CM000674.2:g.25209631del	GRCh38
NC_000012.11:g.25362565del , CM000674.1:g.25362565del	GRCh37
NC_000012.10:g.25253832del	NCBI36
NG_007524.1:g.46298del
NG_007524.2:g.46381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*172del (KRAS)	ENSP00000452512.1:n.*172del
ENST00000685328.1:c.*172del (KRAS)	ENSP00000508921.1:n.*172del
ENST00000686877.1:c.*710del (KRAS)	ENSP00000510431.1:n.*710del
ENST00000687356.1:c.*437del (KRAS)	ENSP00000510511.1:n.*437del
ENST00000688940.1:c.*172del (KRAS)	ENSP00000509238.1:n.*172del
ENST00000690406.1:c.542del (KRAS)
ENST00000690804.1:c.*700del (KRAS)	ENSP00000508568.1:n.*700del
ENST00000692768.1:c.*172del (KRAS)	ENSP00000510254.1:n.*172del
ENST00000693229.1:c.*172del (KRAS)	ENSP00000509223.1:n.*172del
ENST00000256078.10:c.*293del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*293del
ENST00000311936.8:c.*172del (KRAS) MANE Select	ENSP00000308495.3:n.*172del
ENST00000553788.6:c.*368del (ETFRF1)	ENSP00000451938.2:n.*368del
ENST00000256078.8:c.*293del (KRAS)	ENSP00000256078.4:n.*293del
ENST00000311936.7:c.*172del (KRAS)	ENSP00000308495.3:n.*172del
ENST00000553788.5:c.*368del (ETFRF1)	ENSP00000451938.1:n.*368del
ENST00000557334.5:c.*172del (KRAS)	ENSP00000452512.1:n.*172del
NM_004985.4:c.*172del (KRAS)	NP_004976.2:n.*172del
NM_033360.3:c.*293del (KRAS)	NP_203524.1:n.*293del
XM_011520653.1:c.*172del (KRAS)	XP_011518955.1:n.*172del
XM_011520653.3:c.*172del (KRAS)	XP_011518955.1:n.*172del
NM_001369786.1:c.*293del (KRAS)	NP_001356715.1:n.*293del
NM_001369787.1:c.*172del (KRAS)	NP_001356716.1:n.*172del
NM_004985.5:c.*172del (KRAS) MANE Select	NP_004976.2:n.*172del
NM_033360.4:c.*293del (KRAS) MANE Plus Clinical	NP_203524.1:n.*293del