Canonical Allele Identifier: CA2617998716

Gene: KRAS ETFRF1

Linked Data

• gnomAD v4: 12-25206198-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206198G>T , CM000674.2:g.25206198G>T	GRCh38
NC_000012.11:g.25359132G>T , CM000674.1:g.25359132G>T	GRCh37
NC_000012.10:g.25250399G>T	NCBI36
NG_007524.1:g.49723C>A
NG_007524.2:g.49806C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3597C>A (KRAS)	ENSP00000508921.1:n.*3597C>A
ENST00000686877.1:c.*4135C>A (KRAS)	ENSP00000510431.1:n.*4135C>A
ENST00000687356.1:c.*3862C>A (KRAS)	ENSP00000510511.1:n.*3862C>A
ENST00000690406.1:c.3967C>A (KRAS)
ENST00000692768.1:c.*3597C>A (KRAS)	ENSP00000510254.1:n.*3597C>A
ENST00000693229.1:c.*3597C>A (KRAS)	ENSP00000509223.1:n.*3597C>A
ENST00000256078.10:c.*3718C>A (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3718C>A
ENST00000311936.8:c.*3597C>A (KRAS) MANE Select	ENSP00000308495.3:n.*3597C>A
ENST00000553788.6:c.51+2191G>T (ETFRF1)	ENSP00000451938.2:n.51+2191G>T
ENST00000311936.7:c.*3597C>A (KRAS)	ENSP00000308495.3:n.*3597C>A
ENST00000553788.5:c.45+2191G>T (ETFRF1)	ENSP00000451938.1:n.45+2191G>T
NM_004985.4:c.*3597C>A (KRAS)	NP_004976.2:n.*3597C>A
NM_033360.3:c.*3718C>A (KRAS)	NP_203524.1:n.*3718C>A
XM_011520653.1:c.*3597C>A (KRAS)	XP_011518955.1:n.*3597C>A
XM_011520653.3:c.*3597C>A (KRAS)	XP_011518955.1:n.*3597C>A
NM_001369786.1:c.*3718C>A (KRAS)	NP_001356715.1:n.*3718C>A
NM_001369787.1:c.*3597C>A (KRAS)	NP_001356716.1:n.*3597C>A
NM_004985.5:c.*3597C>A (KRAS) MANE Select	NP_004976.2:n.*3597C>A
NM_033360.4:c.*3718C>A (KRAS) MANE Plus Clinical	NP_203524.1:n.*3718C>A