Canonical Allele Identifier: CA2684591480

Gene: MET

Linked Data

• gnomAD v4: 7-116763207-T-TTAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763208_116763211dup , CM000669.2:g.116763208_116763211dup	GRCh38
NC_000007.13:g.116403262_116403265dup , CM000669.1:g.116403262_116403265dup	GRCh37
NC_000007.12:g.116190498_116190501dup	NCBI36
NG_008996.1:g.95804_95807dup , LRG_662:g.95804_95807dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2523_2526dup	ENSP00000398776.2:p.Pro843Ter
ENST00000436117.3:c.*128_*131dup	ENSP00000410980.2:n.*128_*131dup
ENST00000318493.11:c.2577_2580dup	ENSP00000317272.6:p.Pro861Ter
ENST00000397752.8:c.2523_2526dup MANE Select	ENSP00000380860.3:p.Pro843Ter
ENST00000318493.10:c.2577_2580dup	ENSP00000317272.6:p.Pro861Ter
ENST00000397752.7:c.2523_2526dup	ENSP00000380860.3:p.Pro843Ter
ENST00000422097.1:c.363_366dup	ENSP00000398776.1:p.Pro123Ter
NM_000245.2:c.2523_2526dup	NP_000236.2:p.Pro843Ter
NM_001127500.1:c.2577_2580dup , LRG_662t1:c.2577_2580dup	NP_001120972.1:p.Pro861Ter
XM_006715990.2:c.1233_1236dup	XP_006716053.1:p.Pro413Ter
XM_006715991.2:c.1233_1236dup	XP_006716054.1:p.Pro413Ter
XM_011516223.1:c.2580_2583dup	XP_011514525.1:p.Pro862Ter
NM_000245.3:c.2523_2526dup	NP_000236.2:p.Pro843Ter
NM_001127500.2:c.2577_2580dup	NP_001120972.1:p.Pro861Ter
NM_001324401.1:c.2523_2526dup	NP_001311330.1:p.Pro843Ter
NM_001324402.1:c.1233_1236dup	NP_001311331.1:p.Pro413Ter
XR_001744772.1:n.2654_2657dup
NM_001127500.3:c.2577_2580dup	NP_001120972.1:p.Pro861Ter
NM_000245.4:c.2523_2526dup MANE Select	NP_000236.2:p.Pro843Ter
NM_001324401.2:c.2523_2526dup	NP_001311330.1:p.Pro843Ter
NM_001324402.2:c.1233_1236dup	NP_001311331.1:p.Pro413Ter
NM_001324401.3:c.2523_2526dup	NP_001311330.1:p.Pro843Ter