Canonical Allele Identifier: CA10641676

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308112
• ClinVar RCV Id: RCV000318738
• dbSNP Id: rs61763590
• gnomAD v2: 12-25361756-C-A
• gnomAD v3: 12-25208822-C-A
• gnomAD v4: 12-25208822-C-A
• MyVariant Identifiers: chr12:g.25361756C>A (hg19) ; chr12:g.25208822C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208822C>A , CM000674.2:g.25208822C>A	GRCh38
NC_000012.11:g.25361756C>A , CM000674.1:g.25361756C>A	GRCh37
NC_000012.10:g.25253023C>A	NCBI36
NG_007524.1:g.47099G>T
NG_007524.2:g.47182G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*973G>T (KRAS)	ENSP00000508921.1:n.*973G>T
ENST00000686877.1:c.*1511G>T (KRAS)	ENSP00000510431.1:n.*1511G>T
ENST00000687356.1:c.*1238G>T (KRAS)	ENSP00000510511.1:n.*1238G>T
ENST00000688940.1:c.*973G>T (KRAS)	ENSP00000509238.1:n.*973G>T
ENST00000690406.1:c.1343G>T (KRAS)
ENST00000690804.1:c.*1501G>T (KRAS)	ENSP00000508568.1:n.*1501G>T
ENST00000692768.1:c.*973G>T (KRAS)	ENSP00000510254.1:n.*973G>T
ENST00000693229.1:c.*973G>T (KRAS)	ENSP00000509223.1:n.*973G>T
ENST00000256078.10:c.*1094G>T (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1094G>T
ENST00000311936.8:c.*973G>T (KRAS) MANE Select	ENSP00000308495.3:n.*973G>T
ENST00000553788.6:c.52-373C>A (ETFRF1)	ENSP00000451938.2:n.52-373C>A
ENST00000311936.7:c.*973G>T (KRAS)	ENSP00000308495.3:n.*973G>T
ENST00000553788.5:c.46-373C>A (ETFRF1)	ENSP00000451938.1:n.46-373C>A
NM_004985.4:c.*973G>T (KRAS)	NP_004976.2:n.*973G>T
NM_033360.3:c.*1094G>T (KRAS)	NP_203524.1:n.*1094G>T
XM_011520653.1:c.*973G>T (KRAS)	XP_011518955.1:n.*973G>T
XM_011520653.3:c.*973G>T (KRAS)	XP_011518955.1:n.*973G>T
NM_001369786.1:c.*1094G>T (KRAS)	NP_001356715.1:n.*1094G>T
NM_001369787.1:c.*973G>T (KRAS)	NP_001356716.1:n.*973G>T
NM_004985.5:c.*973G>T (KRAS) MANE Select	NP_004976.2:n.*973G>T
NM_033360.4:c.*1094G>T (KRAS) MANE Plus Clinical	NP_203524.1:n.*1094G>T