Canonical Allele Identifier: CA10640713

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308080
• ClinVar RCV Id: RCV000263199
• dbSNP Id: rs886049183
• MyVariant Identifiers: chr12:g.25359581G>A (hg19) ; chr12:g.25206647G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206647G>A , CM000674.2:g.25206647G>A	GRCh38
NC_000012.11:g.25359581G>A , CM000674.1:g.25359581G>A	GRCh37
NC_000012.10:g.25250848G>A	NCBI36
NG_007524.1:g.49274C>T
NG_007524.2:g.49357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3148C>T (KRAS)	ENSP00000508921.1:n.*3148C>T
ENST00000686877.1:c.*3686C>T (KRAS)	ENSP00000510431.1:n.*3686C>T
ENST00000687356.1:c.*3413C>T (KRAS)	ENSP00000510511.1:n.*3413C>T
ENST00000690406.1:c.3518C>T (KRAS)
ENST00000692768.1:c.*3148C>T (KRAS)	ENSP00000510254.1:n.*3148C>T
ENST00000693229.1:c.*3148C>T (KRAS)	ENSP00000509223.1:n.*3148C>T
ENST00000256078.10:c.*3269C>T (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3269C>T
ENST00000311936.8:c.*3148C>T (KRAS) MANE Select	ENSP00000308495.3:n.*3148C>T
ENST00000553788.6:c.52-2548G>A (ETFRF1)	ENSP00000451938.2:n.52-2548G>A
ENST00000311936.7:c.*3148C>T (KRAS)	ENSP00000308495.3:n.*3148C>T
ENST00000553788.5:c.46-2548G>A (ETFRF1)	ENSP00000451938.1:n.46-2548G>A
NM_004985.4:c.*3148C>T (KRAS)	NP_004976.2:n.*3148C>T
NM_033360.3:c.*3269C>T (KRAS)	NP_203524.1:n.*3269C>T
XM_011520653.1:c.*3148C>T (KRAS)	XP_011518955.1:n.*3148C>T
XM_011520653.3:c.*3148C>T (KRAS)	XP_011518955.1:n.*3148C>T
NM_001369786.1:c.*3269C>T (KRAS)	NP_001356715.1:n.*3269C>T
NM_001369787.1:c.*3148C>T (KRAS)	NP_001356716.1:n.*3148C>T
NM_004985.5:c.*3148C>T (KRAS) MANE Select	NP_004976.2:n.*3148C>T
NM_033360.4:c.*3269C>T (KRAS) MANE Plus Clinical	NP_203524.1:n.*3269C>T