Canonical Allele Identifier: CA2617994314

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209757-TGTACTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209761_25209766del , CM000674.2:g.25209761_25209766del	GRCh38
NC_000012.11:g.25362695_25362700del , CM000674.1:g.25362695_25362700del	GRCh37
NC_000012.10:g.25253962_25253967del	NCBI36
NG_007524.1:g.46158_46163del
NG_007524.2:g.46241_46246del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*32_*37del	ENSP00000452512.1:n.*32_*37del
ENST00000685328.1:c.*32_*37del	ENSP00000508921.1:n.*32_*37del
ENST00000686877.1:c.*570_*575del	ENSP00000510431.1:n.*570_*575del
ENST00000687356.1:c.*297_*302del	ENSP00000510511.1:n.*297_*302del
ENST00000688228.1:n.1073_1078del
ENST00000688940.1:c.*32_*37del	ENSP00000509238.1:n.*32_*37del
ENST00000690406.1:c.402_407del
ENST00000690804.1:c.*560_*565del	ENSP00000508568.1:n.*560_*565del
ENST00000692768.1:c.*32_*37del	ENSP00000510254.1:n.*32_*37del
ENST00000693229.1:c.*32_*37del	ENSP00000509223.1:n.*32_*37del
ENST00000256078.10:c.*153_*158del MANE Plus Clinical	ENSP00000256078.5:n.*153_*158del
ENST00000311936.8:c.*32_*37del MANE Select	ENSP00000308495.3:n.*32_*37del
ENST00000256078.8:c.*153_*158del	ENSP00000256078.4:n.*153_*158del
ENST00000311936.7:c.*32_*37del	ENSP00000308495.3:n.*32_*37del
ENST00000557334.5:c.*32_*37del	ENSP00000452512.1:n.*32_*37del
NM_004985.4:c.*32_*37del	NP_004976.2:n.*32_*37del
NM_033360.3:c.*153_*158del	NP_203524.1:n.*153_*158del
XM_011520653.1:c.*32_*37del	XP_011518955.1:n.*32_*37del
XM_011520653.3:c.*32_*37del	XP_011518955.1:n.*32_*37del
NM_001369786.1:c.*153_*158del	NP_001356715.1:n.*153_*158del
NM_001369787.1:c.*32_*37del	NP_001356716.1:n.*32_*37del
NM_004985.5:c.*32_*37del MANE Select	NP_004976.2:n.*32_*37del
NM_033360.4:c.*153_*158del MANE Plus Clinical	NP_203524.1:n.*153_*158del