Canonical Allele Identifier: CA686712812

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1171025213
• MyVariant Identifiers: chr12:g.25359938G>C (hg19) ; chr12:g.25207004G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25207004G>C , CM000674.2:g.25207004G>C	GRCh38
NC_000012.11:g.25359938G>C , CM000674.1:g.25359938G>C	GRCh37
NC_000012.10:g.25251205G>C	NCBI36
NG_007524.1:g.48917C>G
NG_007524.2:g.49000C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000685328.1:c.*2791C>G (KRAS)	ENSP00000508921.1:n.*2791C>G
ENST00000686877.1:c.*3329C>G (KRAS)	ENSP00000510431.1:n.*3329C>G
ENST00000687356.1:c.*3056C>G (KRAS)	ENSP00000510511.1:n.*3056C>G
ENST00000688940.1:c.*2791C>G (KRAS)	ENSP00000509238.1:n.*2791C>G
ENST00000690406.1:c.3161C>G (KRAS)
ENST00000692768.1:c.*2791C>G (KRAS)	ENSP00000510254.1:n.*2791C>G
ENST00000693229.1:c.*2791C>G (KRAS)	ENSP00000509223.1:n.*2791C>G
ENST00000256078.10:c.*2912C>G (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*2912C>G
ENST00000311936.8:c.*2791C>G (KRAS) MANE Select	ENSP00000308495.3:n.*2791C>G
ENST00000553788.6:c.52-2191G>C (ETFRF1)	ENSP00000451938.2:n.52-2191G>C
ENST00000311936.7:c.*2791C>G (KRAS)	ENSP00000308495.3:n.*2791C>G
ENST00000553788.5:c.46-2191G>C (ETFRF1)	ENSP00000451938.1:n.46-2191G>C
NM_004985.4:c.*2791C>G (KRAS)	NP_004976.2:n.*2791C>G
NM_033360.3:c.*2912C>G (KRAS)	NP_203524.1:n.*2912C>G
XM_011520653.1:c.*2791C>G (KRAS)	XP_011518955.1:n.*2791C>G
XM_011520653.3:c.*2791C>G (KRAS)	XP_011518955.1:n.*2791C>G
NM_001369786.1:c.*2912C>G (KRAS)	NP_001356715.1:n.*2912C>G
NM_001369787.1:c.*2791C>G (KRAS)	NP_001356716.1:n.*2791C>G
NM_004985.5:c.*2791C>G (KRAS) MANE Select	NP_004976.2:n.*2791C>G
NM_033360.4:c.*2912C>G (KRAS) MANE Plus Clinical	NP_203524.1:n.*2912C>G