Canonical Allele Identifier: CA603691315

Gene: KRAS

Linked Data

• dbSNP Id: rs1329643600
• gnomAD v2: 12-25362693-T-TACTA
• gnomAD v4: 12-25209759-T-TACTA
• MyVariant Identifiers: chr12:g.25362693_25362694insACTA (hg19) ; chr12:g.25209759_25209760insACTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209760_25209763dup , CM000674.2:g.25209760_25209763dup	GRCh38
NC_000012.11:g.25362694_25362697dup , CM000674.1:g.25362694_25362697dup	GRCh37
NC_000012.10:g.25253961_25253964dup	NCBI36
NG_007524.1:g.46158_46161dup
NG_007524.2:g.46241_46244dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*32_*35dup	ENSP00000452512.1:n.*32_*35dup
ENST00000685328.1:c.*32_*35dup	ENSP00000508921.1:n.*32_*35dup
ENST00000686877.1:c.*570_*573dup	ENSP00000510431.1:n.*570_*573dup
ENST00000687356.1:c.*297_*300dup	ENSP00000510511.1:n.*297_*300dup
ENST00000688228.1:n.1073_1076dup
ENST00000688940.1:c.*32_*35dup	ENSP00000509238.1:n.*32_*35dup
ENST00000690406.1:c.402_405dup
ENST00000690804.1:c.*560_*563dup	ENSP00000508568.1:n.*560_*563dup
ENST00000692768.1:c.*32_*35dup	ENSP00000510254.1:n.*32_*35dup
ENST00000693229.1:c.*32_*35dup	ENSP00000509223.1:n.*32_*35dup
ENST00000256078.10:c.*153_*156dup MANE Plus Clinical	ENSP00000256078.5:n.*153_*156dup
ENST00000311936.8:c.*32_*35dup MANE Select	ENSP00000308495.3:n.*32_*35dup
ENST00000256078.8:c.*153_*156dup	ENSP00000256078.4:n.*153_*156dup
ENST00000311936.7:c.*32_*35dup	ENSP00000308495.3:n.*32_*35dup
ENST00000557334.5:c.*32_*35dup	ENSP00000452512.1:n.*32_*35dup
NM_004985.4:c.*32_*35dup	NP_004976.2:n.*32_*35dup
NM_033360.3:c.*153_*156dup	NP_203524.1:n.*153_*156dup
XM_011520653.1:c.*32_*35dup	XP_011518955.1:n.*32_*35dup
XM_011520653.3:c.*32_*35dup	XP_011518955.1:n.*32_*35dup
NM_001369786.1:c.*153_*156dup	NP_001356715.1:n.*153_*156dup
NM_001369787.1:c.*32_*35dup	NP_001356716.1:n.*32_*35dup
NM_004985.5:c.*32_*35dup MANE Select	NP_004976.2:n.*32_*35dup
NM_033360.4:c.*153_*156dup MANE Plus Clinical	NP_203524.1:n.*153_*156dup