Canonical Allele Identifier: CA2684591314

Gene: MET

Linked Data

• gnomAD v4: 7-116759489-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759491del , CM000669.2:g.116759491del	GRCh38
NC_000007.13:g.116399545del , CM000669.1:g.116399545del	GRCh37
NC_000007.12:g.116186781del	NCBI36
NG_008996.1:g.92087del , LRG_662:g.92087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2364+1del
ENST00000436117.3:c.2264+871del	ENSP00000410980.2:n.2264+871del
ENST00000318493.11:c.2418+1del
ENST00000397752.8:c.2364+1del
ENST00000318493.10:c.2418+1del
ENST00000397752.7:c.2364+1del
ENST00000422097.1:c.204+1del
ENST00000436117.2:c.2264+871del	ENSP00000410980.2:n.2264+871del
NM_000245.2:c.2364+1del
NM_001127500.1:c.2418+1del , LRG_662t1:c.2418+1del
XM_006715990.2:c.1074+1del
XM_006715991.2:c.1074+1del
XM_011516223.1:c.2421+1del
NM_000245.3:c.2364+1del
NM_001127500.2:c.2418+1del
NM_001324401.1:c.2364+1del
NM_001324402.1:c.1074+1del
XR_001744772.1:n.2495+871del
NM_001127500.3:c.2418+1del
NM_000245.4:c.2364+1del
NM_001324401.2:c.2364+1del
NM_001324402.2:c.1074+1del
NM_001324401.3:c.2364+1del