Canonical Allele Identifier: CA164867523

Gene: MET COMETT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116672511G>T , CM000669.2:g.116672511G>T	GRCh38
NC_000007.13:g.116312565G>T , CM000669.1:g.116312565G>T	GRCh37
NC_000007.12:g.116099801G>T	NCBI36
NG_008996.1:g.5107G>T , LRG_662:g.5107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.-81G>T (MET)	ENSP00000398776.2:n.-81G>T
ENST00000436117.3:c.-81G>T (MET)	ENSP00000410980.2:n.-81G>T
ENST00000318493.11:c.-81G>T (MET)	ENSP00000317272.6:n.-81G>T
ENST00000397752.8:c.-81G>T (MET) MANE Select	ENSP00000380860.3:n.-81G>T
ENST00000318493.10:c.-81G>T (MET)	ENSP00000317272.6:n.-81G>T
ENST00000397752.7:c.-81G>T (MET)	ENSP00000380860.3:n.-81G>T
ENST00000456159.1:c.-74G>T (MET)	ENSP00000413857.1:n.-74G>T
NM_000245.2:c.-81G>T (MET)	NP_000236.2:n.-81G>T
NM_001127500.1:c.-81G>T , LRG_662t1:c.-81G>T (MET)	NP_001120972.1:n.-81G>T
XM_006715991.2:c.-157G>T (MET)	XP_006716054.1:n.-157G>T
XM_011516223.1:c.-74G>T (MET)	XP_011514525.1:n.-74G>T
NM_000245.3:c.-81G>T (MET)	NP_000236.2:n.-81G>T
NM_001127500.2:c.-81G>T (MET)	NP_001120972.1:n.-81G>T
NM_001324401.1:c.-81G>T (MET)	NP_001311330.1:n.-81G>T
NM_001324402.1:c.-157G>T (MET)	NP_001311331.1:n.-157G>T
XR_001744772.1:n.101G>T (MET)
NM_001127500.3:c.-81G>T (MET)	NP_001120972.1:n.-81G>T
NM_000245.4:c.-81G>T (MET) MANE Select	NP_000236.2:n.-81G>T
NM_001324401.2:c.-81G>T (MET)	NP_001311330.1:n.-81G>T
NM_001324402.2:c.-157G>T (MET)	NP_001311331.1:n.-157G>T
NR_165032.1:n.88-8470C>A (COMETT)
NR_165033.1:n.88-8470C>A (COMETT)
NM_001324401.3:c.-81G>T (MET)	NP_001311330.1:n.-81G>T