Canonical Allele Identifier: CA2580617087

Gene: MET

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116741036_116741037del , CM000669.2:g.116741036_116741037del	GRCh38
NC_000007.13:g.116381090_116381091del , CM000669.1:g.116381090_116381091del	GRCh37
NC_000007.12:g.116168326_116168327del	NCBI36
NG_008996.1:g.73632_73633del , LRG_662:g.73632_73633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1701+11_1701+12del	ENSP00000398776.2:n.1701+11_1701+12del
ENST00000436117.3:c.1701+11_1701+12del	ENSP00000410980.2:n.1701+11_1701+12del
ENST00000318493.11:c.1701+11_1701+12del	ENSP00000317272.6:n.1701+11_1701+12del
ENST00000397752.8:c.1701+11_1701+12del MANE Select	ENSP00000380860.3:n.1701+11_1701+12del
ENST00000318493.10:c.1701+11_1701+12del	ENSP00000317272.6:n.1701+11_1701+12del
ENST00000397752.7:c.1701+11_1701+12del	ENSP00000380860.3:n.1701+11_1701+12del
ENST00000436117.2:c.1701+11_1701+12del	ENSP00000410980.2:n.1701+11_1701+12del
ENST00000495962.1:n.681+11_681+12del
NM_000245.2:c.1701+11_1701+12del	NP_000236.2:n.1701+11_1701+12del
NM_001127500.1:c.1701+11_1701+12del , LRG_662t1:c.1701+11_1701+12del	NP_001120972.1:n.1701+11_1701+12del
XM_006715990.2:c.411+11_411+12del	XP_006716053.1:n.411+11_411+12del
XM_006715991.2:c.411+11_411+12del	XP_006716054.1:n.411+11_411+12del
XM_011516223.1:c.1758+11_1758+12del	XP_011514525.1:n.1758+11_1758+12del
NM_000245.3:c.1701+11_1701+12del	NP_000236.2:n.1701+11_1701+12del
NM_001127500.2:c.1701+11_1701+12del	NP_001120972.1:n.1701+11_1701+12del
NM_001324401.1:c.1701+11_1701+12del	NP_001311330.1:n.1701+11_1701+12del
NM_001324402.1:c.411+11_411+12del	NP_001311331.1:n.411+11_411+12del
XR_001744772.1:n.1932+11_1932+12del
NM_001127500.3:c.1701+11_1701+12del	NP_001120972.1:n.1701+11_1701+12del
NM_000245.4:c.1701+11_1701+12del MANE Select	NP_000236.2:n.1701+11_1701+12del
NM_001324401.2:c.1701+11_1701+12del	NP_001311330.1:n.1701+11_1701+12del
NM_001324402.2:c.411+11_411+12del	NP_001311331.1:n.411+11_411+12del
NM_001324401.3:c.1701+11_1701+12del	NP_001311330.1:n.1701+11_1701+12del