Canonical Allele Identifier: CA2617994318

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209758-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209758G>T , CM000674.2:g.25209758G>T	GRCh38
NC_000012.11:g.25362692G>T , CM000674.1:g.25362692G>T	GRCh37
NC_000012.10:g.25253959G>T	NCBI36
NG_007524.1:g.46163C>A
NG_007524.2:g.46246C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*37C>A	ENSP00000452512.1:n.*37C>A
ENST00000685328.1:c.*37C>A	ENSP00000508921.1:n.*37C>A
ENST00000686877.1:c.*575C>A	ENSP00000510431.1:n.*575C>A
ENST00000687356.1:c.*302C>A	ENSP00000510511.1:n.*302C>A
ENST00000688228.1:n.1078C>A
ENST00000688940.1:c.*37C>A	ENSP00000509238.1:n.*37C>A
ENST00000690406.1:c.407C>A
ENST00000690804.1:c.*565C>A	ENSP00000508568.1:n.*565C>A
ENST00000692768.1:c.*37C>A	ENSP00000510254.1:n.*37C>A
ENST00000693229.1:c.*37C>A	ENSP00000509223.1:n.*37C>A
ENST00000256078.10:c.*158C>A MANE Plus Clinical	ENSP00000256078.5:n.*158C>A
ENST00000311936.8:c.*37C>A MANE Select	ENSP00000308495.3:n.*37C>A
ENST00000256078.8:c.*158C>A	ENSP00000256078.4:n.*158C>A
ENST00000311936.7:c.*37C>A	ENSP00000308495.3:n.*37C>A
ENST00000557334.5:c.*37C>A	ENSP00000452512.1:n.*37C>A
NM_004985.4:c.*37C>A	NP_004976.2:n.*37C>A
NM_033360.3:c.*158C>A	NP_203524.1:n.*158C>A
XM_011520653.1:c.*37C>A	XP_011518955.1:n.*37C>A
XM_011520653.3:c.*37C>A	XP_011518955.1:n.*37C>A
NM_001369786.1:c.*158C>A	NP_001356715.1:n.*158C>A
NM_001369787.1:c.*37C>A	NP_001356716.1:n.*37C>A
NM_004985.5:c.*37C>A MANE Select	NP_004976.2:n.*37C>A
NM_033360.4:c.*158C>A MANE Plus Clinical	NP_203524.1:n.*158C>A