Canonical Allele Identifier: CA603690992

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs71065923
• gnomAD v2: 12-25361101-T-TAA
• gnomAD v3: 12-25208167-T-TAA
• gnomAD v4: 12-25208167-T-TAA
• MyVariant Identifiers: chr12:g.25361102_25361103insAA (hg19) ; chr12:g.25361101_25361102insAA (hg19) ; chr12:g.25208168_25208169insAA (hg38) ; chr12:g.25208167_25208168insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208178_25208179dup , CM000674.2:g.25208178_25208179dup	GRCh38
NC_000012.11:g.25361112_25361113dup , CM000674.1:g.25361112_25361113dup	GRCh37
NC_000012.10:g.25252379_25252380dup	NCBI36
NG_007524.1:g.47752_47753dup
NG_007524.2:g.47835_47836dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1626_*1627dup (KRAS)	ENSP00000508921.1:n.*1626_*1627dup
ENST00000686877.1:c.*2164_*2165dup (KRAS)	ENSP00000510431.1:n.*2164_*2165dup
ENST00000687356.1:c.*1891_*1892dup (KRAS)	ENSP00000510511.1:n.*1891_*1892dup
ENST00000688940.1:c.*1626_*1627dup (KRAS)	ENSP00000509238.1:n.*1626_*1627dup
ENST00000690406.1:c.1996_1997dup (KRAS)
ENST00000690804.1:c.*2154_*2155dup (KRAS)	ENSP00000508568.1:n.*2154_*2155dup
ENST00000692768.1:c.*1626_*1627dup (KRAS)	ENSP00000510254.1:n.*1626_*1627dup
ENST00000693229.1:c.*1626_*1627dup (KRAS)	ENSP00000509223.1:n.*1626_*1627dup
ENST00000256078.10:c.*1747_*1748dup (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1747_*1748dup
ENST00000311936.8:c.*1626_*1627dup (KRAS) MANE Select	ENSP00000308495.3:n.*1626_*1627dup
ENST00000553788.6:c.52-1017_52-1016dup (ETFRF1)	ENSP00000451938.2:n.52-1017_52-1016dup
ENST00000311936.7:c.*1626_*1627dup (KRAS)	ENSP00000308495.3:n.*1626_*1627dup
ENST00000553788.5:c.46-1017_46-1016dup (ETFRF1)	ENSP00000451938.1:n.46-1017_46-1016dup
NM_004985.4:c.*1626_*1627dup (KRAS)	NP_004976.2:n.*1626_*1627dup
NM_033360.3:c.*1747_*1748dup (KRAS)	NP_203524.1:n.*1747_*1748dup
XM_011520653.1:c.*1626_*1627dup (KRAS)	XP_011518955.1:n.*1626_*1627dup
XM_011520653.3:c.*1626_*1627dup (KRAS)	XP_011518955.1:n.*1626_*1627dup
NM_001369786.1:c.*1747_*1748dup (KRAS)	NP_001356715.1:n.*1747_*1748dup
NM_001369787.1:c.*1626_*1627dup (KRAS)	NP_001356716.1:n.*1626_*1627dup
NM_004985.5:c.*1626_*1627dup (KRAS) MANE Select	NP_004976.2:n.*1626_*1627dup
NM_033360.4:c.*1747_*1748dup (KRAS) MANE Plus Clinical	NP_203524.1:n.*1747_*1748dup