Canonical Allele Identifier: CA256991

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116778827T>C , CM000669.2:g.116778827T>C	GRCh38
NC_000007.13:g.116418881T>C , CM000669.1:g.116418881T>C	GRCh37
NC_000007.12:g.116206117T>C	NCBI36
NG_008996.1:g.111423T>C , LRG_662:g.111423T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3392T>C MANE Select	NP_000236.2:p.Met1131Thr
ENST00000397752.8:c.3392T>C MANE Select	ENSP00000380860.3:p.Met1131Thr
NM_000245.2:c.3392T>C	NP_000236.2:p.Met1131Thr
NM_000245.3:c.3392T>C	NP_000236.2:p.Met1131Thr
NM_001127500.1:c.3446T>C , LRG_662t1:c.3446T>C	NP_001120972.1:p.Met1149Thr
NM_001127500.2:c.3446T>C	NP_001120972.1:p.Met1149Thr
NM_001127500.3:c.3446T>C	NP_001120972.1:p.Met1149Thr
NM_001324402.1:c.2102T>C	NP_001311331.1:p.Met701Thr
NM_001324402.2:c.2102T>C	NP_001311331.1:p.Met701Thr
ENST00000318493.10:c.3446T>C	ENSP00000317272.6:p.Met1149Thr
ENST00000318493.11:c.3446T>C	ENSP00000317272.6:p.Met1149Thr
ENST00000397752.7:c.3392T>C	ENSP00000380860.3:p.Met1131Thr
ENST00000436117.3:c.*997T>C	ENSP00000410980.2:n.*997T>C
XM_006715990.2:c.2102T>C	XP_006716053.1:p.Met701Thr
XM_006715991.2:c.2102T>C	XP_006716054.1:p.Met701Thr
XM_011516223.1:c.3449T>C	XP_011514525.1:p.Met1150Thr
XR_001744772.1:n.3523T>C