Canonical Allele Identifier: CA2700087244

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771922_116771925del , CM000669.2:g.116771922_116771925del	GRCh38
NC_000007.13:g.116411976_116411979del , CM000669.1:g.116411976_116411979del	GRCh37
NC_000007.12:g.116199212_116199215del	NCBI36
NG_008996.1:g.104518_104521del , LRG_662:g.104518_104521del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*566_*569del	ENSP00000410980.2:n.*566_*569del
ENST00000318493.11:c.3015_3018del	ENSP00000317272.6:p.Ser1006Ter
ENST00000397752.8:c.2961_2964del MANE Select	ENSP00000380860.3:p.Ser988Ter
ENST00000318493.10:c.3015_3018del	ENSP00000317272.6:p.Ser1006Ter
ENST00000397752.7:c.2961_2964del	ENSP00000380860.3:p.Ser988Ter
ENST00000454623.1:c.283+268_283+271del	ENSP00000398140.1:n.283+268_283+271del
NM_000245.2:c.2961_2964del	NP_000236.2:p.Ser988Ter
NM_001127500.1:c.3015_3018del , LRG_662t1:c.3015_3018del	NP_001120972.1:p.Ser1006Ter
XM_006715990.2:c.1671_1674del	XP_006716053.1:p.Ser558Ter
XM_006715991.2:c.1671_1674del	XP_006716054.1:p.Ser558Ter
XM_011516223.1:c.3018_3021del	XP_011514525.1:p.Ser1007Ter
NM_000245.3:c.2961_2964del	NP_000236.2:p.Ser988Ter
NM_001127500.2:c.3015_3018del	NP_001120972.1:p.Ser1006Ter
NM_001324402.1:c.1671_1674del	NP_001311331.1:p.Ser558Ter
XR_001744772.1:n.3092_3095del
NM_001127500.3:c.3015_3018del	NP_001120972.1:p.Ser1006Ter
NM_000245.4:c.2961_2964del MANE Select	NP_000236.2:p.Ser988Ter
NM_001324402.2:c.1671_1674del	NP_001311331.1:p.Ser558Ter