Canonical Allele Identifier: CA1139532614

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771911del , CM000669.2:g.116771911del	GRCh38
NC_000007.13:g.116411965del , CM000669.1:g.116411965del	GRCh37
NC_000007.12:g.116199201del	NCBI36
NG_008996.1:g.104507del , LRG_662:g.104507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*555del	ENSP00000410980.2:n.*555del
ENST00000318493.11:c.3004del	ENSP00000317272.6:p.Val1002Ter
ENST00000397752.8:c.2950del MANE Select	ENSP00000380860.3:p.Val984Ter
ENST00000318493.10:c.3004del	ENSP00000317272.6:p.Val1002Ter
ENST00000397752.7:c.2950del	ENSP00000380860.3:p.Val984Ter
ENST00000454623.1:c.283+257del	ENSP00000398140.1:n.283+257del
NM_000245.2:c.2950del	NP_000236.2:p.Val984Ter
NM_001127500.1:c.3004del , LRG_662t1:c.3004del	NP_001120972.1:p.Val1002Ter
XM_006715990.2:c.1660del	XP_006716053.1:p.Val554Ter
XM_006715991.2:c.1660del	XP_006716054.1:p.Val554Ter
XM_011516223.1:c.3007del	XP_011514525.1:p.Val1003Ter
NM_000245.3:c.2950del	NP_000236.2:p.Val984Ter
NM_001127500.2:c.3004del	NP_001120972.1:p.Val1002Ter
NM_001324402.1:c.1660del	NP_001311331.1:p.Val554Ter
XR_001744772.1:n.3081del
NM_001127500.3:c.3004del	NP_001120972.1:p.Val1002Ter
NM_000245.4:c.2950del MANE Select	NP_000236.2:p.Val984Ter
NM_001324402.2:c.1660del	NP_001311331.1:p.Val554Ter