Canonical Allele Identifier: CA10632479

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308101
• ClinVar RCV Id: RCV000264327 ; RCV000359373 ; RCV003389785
• dbSNP Id: rs535478558
• gnomAD v2: 12-25361090-TTA-T
• gnomAD v3: 12-25208156-TTA-T
• gnomAD v4: 12-25208156-TTA-T
• MyVariant Identifiers: chr12:g.25361091_25361092del (hg19) ; chr12:g.25208157_25208158del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208157_25208158del , CM000674.2:g.25208157_25208158del	GRCh38
NC_000012.11:g.25361091_25361092del , CM000674.1:g.25361091_25361092del	GRCh37
NC_000012.10:g.25252358_25252359del	NCBI36
NG_007524.1:g.47763_47764del
NG_007524.2:g.47846_47847del

Transcript Alleles

HGVS	Amino-acid change
ENST00000685328.1:c.*1637_*1638del (KRAS)	ENSP00000508921.1:n.*1637_*1638del
ENST00000686877.1:c.*2175_*2176del (KRAS)	ENSP00000510431.1:n.*2175_*2176del
ENST00000687356.1:c.*1902_*1903del (KRAS)	ENSP00000510511.1:n.*1902_*1903del
ENST00000688940.1:c.*1637_*1638del (KRAS)	ENSP00000509238.1:n.*1637_*1638del
ENST00000690406.1:c.2007_2008del (KRAS)
ENST00000690804.1:c.*2165_*2166del (KRAS)	ENSP00000508568.1:n.*2165_*2166del
ENST00000692768.1:c.*1637_*1638del (KRAS)	ENSP00000510254.1:n.*1637_*1638del
ENST00000693229.1:c.*1637_*1638del (KRAS)	ENSP00000509223.1:n.*1637_*1638del
ENST00000256078.10:c.*1758_*1759del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1758_*1759del
ENST00000311936.8:c.*1637_*1638del (KRAS) MANE Select	ENSP00000308495.3:n.*1637_*1638del
ENST00000553788.6:c.52-1038_52-1037del (ETFRF1)	ENSP00000451938.2:n.52-1038_52-1037del
ENST00000311936.7:c.*1637_*1638del (KRAS)	ENSP00000308495.3:n.*1637_*1638del
ENST00000553788.5:c.46-1038_46-1037del (ETFRF1)	ENSP00000451938.1:n.46-1038_46-1037del
NM_004985.4:c.*1637_*1638del (KRAS)	NP_004976.2:n.*1637_*1638del
NM_033360.3:c.*1758_*1759del (KRAS)	NP_203524.1:n.*1758_*1759del
XM_011520653.1:c.*1637_*1638del (KRAS)	XP_011518955.1:n.*1637_*1638del
XM_011520653.3:c.*1637_*1638del (KRAS)	XP_011518955.1:n.*1637_*1638del
NM_001369786.1:c.*1758_*1759del (KRAS)	NP_001356715.1:n.*1758_*1759del
NM_001369787.1:c.*1637_*1638del (KRAS)	NP_001356716.1:n.*1637_*1638del
NM_004985.5:c.*1637_*1638del (KRAS) MANE Select	NP_004976.2:n.*1637_*1638del
NM_033360.4:c.*1758_*1759del (KRAS) MANE Plus Clinical	NP_203524.1:n.*1758_*1759del