Canonical Allele Identifier: CA2617994200

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209647-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209647T>G , CM000674.2:g.25209647T>G	GRCh38
NC_000012.11:g.25362581T>G , CM000674.1:g.25362581T>G	GRCh37
NC_000012.10:g.25253848T>G	NCBI36
NG_007524.1:g.46274A>C
NG_007524.2:g.46357A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*148A>C	ENSP00000452512.1:n.*148A>C
ENST00000685328.1:c.*148A>C	ENSP00000508921.1:n.*148A>C
ENST00000686877.1:c.*686A>C	ENSP00000510431.1:n.*686A>C
ENST00000687356.1:c.*413A>C	ENSP00000510511.1:n.*413A>C
ENST00000688940.1:c.*148A>C	ENSP00000509238.1:n.*148A>C
ENST00000690406.1:c.518A>C
ENST00000690804.1:c.*676A>C	ENSP00000508568.1:n.*676A>C
ENST00000692768.1:c.*148A>C	ENSP00000510254.1:n.*148A>C
ENST00000693229.1:c.*148A>C	ENSP00000509223.1:n.*148A>C
ENST00000256078.10:c.*269A>C MANE Plus Clinical	ENSP00000256078.5:n.*269A>C
ENST00000311936.8:c.*148A>C MANE Select	ENSP00000308495.3:n.*148A>C
ENST00000256078.8:c.*269A>C	ENSP00000256078.4:n.*269A>C
ENST00000311936.7:c.*148A>C	ENSP00000308495.3:n.*148A>C
ENST00000557334.5:c.*148A>C	ENSP00000452512.1:n.*148A>C
NM_004985.4:c.*148A>C	NP_004976.2:n.*148A>C
NM_033360.3:c.*269A>C	NP_203524.1:n.*269A>C
XM_011520653.1:c.*148A>C	XP_011518955.1:n.*148A>C
XM_011520653.3:c.*148A>C	XP_011518955.1:n.*148A>C
NM_001369786.1:c.*269A>C	NP_001356715.1:n.*269A>C
NM_001369787.1:c.*148A>C	NP_001356716.1:n.*148A>C
NM_004985.5:c.*148A>C MANE Select	NP_004976.2:n.*148A>C
NM_033360.4:c.*269A>C MANE Plus Clinical	NP_203524.1:n.*269A>C