Canonical Allele Identifier: CA603691013

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1176480188
• gnomAD v2: 12-25361165-T-A
• MyVariant Identifiers: chr12:g.25361165T>A (hg19) ; chr12:g.25208231T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208231T>A , CM000674.2:g.25208231T>A	GRCh38
NC_000012.11:g.25361165T>A , CM000674.1:g.25361165T>A	GRCh37
NC_000012.10:g.25252432T>A	NCBI36
NG_007524.1:g.47690A>T
NG_007524.2:g.47773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1564A>T (KRAS)	ENSP00000508921.1:n.*1564A>T
ENST00000686877.1:c.*2102A>T (KRAS)	ENSP00000510431.1:n.*2102A>T
ENST00000687356.1:c.*1829A>T (KRAS)	ENSP00000510511.1:n.*1829A>T
ENST00000688940.1:c.*1564A>T (KRAS)	ENSP00000509238.1:n.*1564A>T
ENST00000690406.1:c.1934A>T (KRAS)
ENST00000690804.1:c.*2092A>T (KRAS)	ENSP00000508568.1:n.*2092A>T
ENST00000692768.1:c.*1564A>T (KRAS)	ENSP00000510254.1:n.*1564A>T
ENST00000693229.1:c.*1564A>T (KRAS)	ENSP00000509223.1:n.*1564A>T
ENST00000256078.10:c.*1685A>T (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1685A>T
ENST00000311936.8:c.*1564A>T (KRAS) MANE Select	ENSP00000308495.3:n.*1564A>T
ENST00000553788.6:c.52-964T>A (ETFRF1)	ENSP00000451938.2:n.52-964T>A
ENST00000311936.7:c.*1564A>T (KRAS)	ENSP00000308495.3:n.*1564A>T
ENST00000553788.5:c.46-964T>A (ETFRF1)	ENSP00000451938.1:n.46-964T>A
NM_004985.4:c.*1564A>T (KRAS)	NP_004976.2:n.*1564A>T
NM_033360.3:c.*1685A>T (KRAS)	NP_203524.1:n.*1685A>T
XM_011520653.1:c.*1564A>T (KRAS)	XP_011518955.1:n.*1564A>T
XM_011520653.3:c.*1564A>T (KRAS)	XP_011518955.1:n.*1564A>T
NM_001369786.1:c.*1685A>T (KRAS)	NP_001356715.1:n.*1685A>T
NM_001369787.1:c.*1564A>T (KRAS)	NP_001356716.1:n.*1564A>T
NM_004985.5:c.*1564A>T (KRAS) MANE Select	NP_004976.2:n.*1564A>T
NM_033360.4:c.*1685A>T (KRAS) MANE Plus Clinical	NP_203524.1:n.*1685A>T