Canonical Allele Identifier: CA603690996

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1555192234
• gnomAD v2: 12-25361101-T-TTAA
• gnomAD v3: 12-25208167-T-TTAA
• gnomAD v4: 12-25208167-T-TTAA
• MyVariant Identifiers: chr12:g.25361101_25361102insTAA (hg19) ; chr12:g.25361102delinsTAAA (hg19) ; chr12:g.25208167_25208168insTAA (hg38) ; chr12:g.25208168delinsTAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208167_25208168insTAA , CM000674.2:g.25208167_25208168insTAA	GRCh38
NC_000012.11:g.25361101_25361102insTAA , CM000674.1:g.25361101_25361102insTAA	GRCh37
NC_000012.10:g.25252368_25252369insTAA	NCBI36
NG_007524.1:g.47753_47754insTTA
NG_007524.2:g.47836_47837insTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1627_*1628insTTA (KRAS)	ENSP00000508921.1:n.*1627_*1628insTTA
ENST00000686877.1:c.*2165_*2166insTTA (KRAS)	ENSP00000510431.1:n.*2165_*2166insTTA
ENST00000687356.1:c.*1892_*1893insTTA (KRAS)	ENSP00000510511.1:n.*1892_*1893insTTA
ENST00000688940.1:c.*1627_*1628insTTA (KRAS)	ENSP00000509238.1:n.*1627_*1628insTTA
ENST00000690406.1:c.1997_1998insTTA (KRAS)
ENST00000690804.1:c.*2155_*2156insTTA (KRAS)	ENSP00000508568.1:n.*2155_*2156insTTA
ENST00000692768.1:c.*1627_*1628insTTA (KRAS)	ENSP00000510254.1:n.*1627_*1628insTTA
ENST00000693229.1:c.*1627_*1628insTTA (KRAS)	ENSP00000509223.1:n.*1627_*1628insTTA
ENST00000256078.10:c.*1748_*1749insTTA (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1748_*1749insTTA
ENST00000311936.8:c.*1627_*1628insTTA (KRAS) MANE Select	ENSP00000308495.3:n.*1627_*1628insTTA
ENST00000553788.6:c.52-1028_52-1027insTAA (ETFRF1)	ENSP00000451938.2:n.52-1028_52-1027insTAA
ENST00000311936.7:c.*1627_*1628insTTA (KRAS)	ENSP00000308495.3:n.*1627_*1628insTTA
ENST00000553788.5:c.46-1028_46-1027insTAA (ETFRF1)	ENSP00000451938.1:n.46-1028_46-1027insTAA
NM_004985.4:c.*1627_*1628insTTA (KRAS)	NP_004976.2:n.*1627_*1628insTTA
NM_033360.3:c.*1748_*1749insTTA (KRAS)	NP_203524.1:n.*1748_*1749insTTA
XM_011520653.1:c.*1627_*1628insTTA (KRAS)	XP_011518955.1:n.*1627_*1628insTTA
XM_011520653.3:c.*1627_*1628insTTA (KRAS)	XP_011518955.1:n.*1627_*1628insTTA
NM_001369786.1:c.*1748_*1749insTTA (KRAS)	NP_001356715.1:n.*1748_*1749insTTA
NM_001369787.1:c.*1627_*1628insTTA (KRAS)	NP_001356716.1:n.*1627_*1628insTTA
NM_004985.5:c.*1627_*1628insTTA (KRAS) MANE Select	NP_004976.2:n.*1627_*1628insTTA
NM_033360.4:c.*1748_*1749insTTA (KRAS) MANE Plus Clinical	NP_203524.1:n.*1748_*1749insTTA