Canonical Allele Identifier: CA2617994087

Gene: KRAS ETFRF1

Linked Data

• gnomAD v4: 12-25209604-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209604G>A , CM000674.2:g.25209604G>A	GRCh38
NC_000012.11:g.25362538G>A , CM000674.1:g.25362538G>A	GRCh37
NC_000012.10:g.25253805G>A	NCBI36
NG_007524.1:g.46317C>T
NG_007524.2:g.46400C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*191C>T (KRAS)	ENSP00000452512.1:n.*191C>T
ENST00000685328.1:c.*191C>T (KRAS)	ENSP00000508921.1:n.*191C>T
ENST00000686877.1:c.*729C>T (KRAS)	ENSP00000510431.1:n.*729C>T
ENST00000687356.1:c.*456C>T (KRAS)	ENSP00000510511.1:n.*456C>T
ENST00000688940.1:c.*191C>T (KRAS)	ENSP00000509238.1:n.*191C>T
ENST00000690406.1:c.561C>T (KRAS)
ENST00000690804.1:c.*719C>T (KRAS)	ENSP00000508568.1:n.*719C>T
ENST00000692768.1:c.*191C>T (KRAS)	ENSP00000510254.1:n.*191C>T
ENST00000693229.1:c.*191C>T (KRAS)	ENSP00000509223.1:n.*191C>T
ENST00000256078.10:c.*312C>T (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*312C>T
ENST00000311936.8:c.*191C>T (KRAS) MANE Select	ENSP00000308495.3:n.*191C>T
ENST00000553788.6:c.*341G>A (ETFRF1)	ENSP00000451938.2:n.*341G>A
ENST00000256078.8:c.*312C>T (KRAS)	ENSP00000256078.4:n.*312C>T
ENST00000311936.7:c.*191C>T (KRAS)	ENSP00000308495.3:n.*191C>T
ENST00000553788.5:c.*341G>A (ETFRF1)	ENSP00000451938.1:n.*341G>A
ENST00000557334.5:c.*191C>T (KRAS)	ENSP00000452512.1:n.*191C>T
NM_004985.4:c.*191C>T (KRAS)	NP_004976.2:n.*191C>T
NM_033360.3:c.*312C>T (KRAS)	NP_203524.1:n.*312C>T
XM_011520653.1:c.*191C>T (KRAS)	XP_011518955.1:n.*191C>T
XM_011520653.3:c.*191C>T (KRAS)	XP_011518955.1:n.*191C>T
NM_001369786.1:c.*312C>T (KRAS)	NP_001356715.1:n.*312C>T
NM_001369787.1:c.*191C>T (KRAS)	NP_001356716.1:n.*191C>T
NM_004985.5:c.*191C>T (KRAS) MANE Select	NP_004976.2:n.*191C>T
NM_033360.4:c.*312C>T (KRAS) MANE Plus Clinical	NP_203524.1:n.*312C>T