Canonical Allele Identifier: CA10632491

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308122
• ClinVar RCV Id: RCV000269265
• dbSNP Id: rs886049197
• gnomAD v2: 12-25362553-G-A
• gnomAD v3: 12-25209619-G-A
• gnomAD v4: 12-25209619-G-A
• MyVariant Identifiers: chr12:g.25362553G>A (hg19) ; chr12:g.25209619G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209619G>A , CM000674.2:g.25209619G>A	GRCh38
NC_000012.11:g.25362553G>A , CM000674.1:g.25362553G>A	GRCh37
NC_000012.10:g.25253820G>A	NCBI36
NG_007524.1:g.46302C>T
NG_007524.2:g.46385C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*176C>T (KRAS)	ENSP00000452512.1:n.*176C>T
ENST00000685328.1:c.*176C>T (KRAS)	ENSP00000508921.1:n.*176C>T
ENST00000686877.1:c.*714C>T (KRAS)	ENSP00000510431.1:n.*714C>T
ENST00000687356.1:c.*441C>T (KRAS)	ENSP00000510511.1:n.*441C>T
ENST00000688940.1:c.*176C>T (KRAS)	ENSP00000509238.1:n.*176C>T
ENST00000690406.1:c.546C>T (KRAS)
ENST00000690804.1:c.*704C>T (KRAS)	ENSP00000508568.1:n.*704C>T
ENST00000692768.1:c.*176C>T (KRAS)	ENSP00000510254.1:n.*176C>T
ENST00000693229.1:c.*176C>T (KRAS)	ENSP00000509223.1:n.*176C>T
ENST00000256078.10:c.*297C>T (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*297C>T
ENST00000311936.8:c.*176C>T (KRAS) MANE Select	ENSP00000308495.3:n.*176C>T
ENST00000553788.6:c.*356G>A (ETFRF1)	ENSP00000451938.2:n.*356G>A
ENST00000256078.8:c.*297C>T (KRAS)	ENSP00000256078.4:n.*297C>T
ENST00000311936.7:c.*176C>T (KRAS)	ENSP00000308495.3:n.*176C>T
ENST00000553788.5:c.*356G>A (ETFRF1)	ENSP00000451938.1:n.*356G>A
ENST00000557334.5:c.*176C>T (KRAS)	ENSP00000452512.1:n.*176C>T
NM_004985.4:c.*176C>T (KRAS)	NP_004976.2:n.*176C>T
NM_033360.3:c.*297C>T (KRAS)	NP_203524.1:n.*297C>T
XM_011520653.1:c.*176C>T (KRAS)	XP_011518955.1:n.*176C>T
XM_011520653.3:c.*176C>T (KRAS)	XP_011518955.1:n.*176C>T
NM_001369786.1:c.*297C>T (KRAS)	NP_001356715.1:n.*297C>T
NM_001369787.1:c.*176C>T (KRAS)	NP_001356716.1:n.*176C>T
NM_004985.5:c.*176C>T (KRAS) MANE Select	NP_004976.2:n.*176C>T
NM_033360.4:c.*297C>T (KRAS) MANE Plus Clinical	NP_203524.1:n.*297C>T