Canonical Allele Identifier: CA2684591321

Gene: MET

Linked Data

• gnomAD v4: 7-116759525-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759526dup , CM000669.2:g.116759526dup	GRCh38
NC_000007.13:g.116399580dup , CM000669.1:g.116399580dup	GRCh37
NC_000007.12:g.116186816dup	NCBI36
NG_008996.1:g.92122dup , LRG_662:g.92122dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2364+36dup	ENSP00000398776.2:n.2364+36dup
ENST00000436117.3:c.2264+906dup	ENSP00000410980.2:n.2264+906dup
ENST00000318493.11:c.2418+36dup	ENSP00000317272.6:n.2418+36dup
ENST00000397752.8:c.2364+36dup MANE Select	ENSP00000380860.3:n.2364+36dup
ENST00000318493.10:c.2418+36dup	ENSP00000317272.6:n.2418+36dup
ENST00000397752.7:c.2364+36dup	ENSP00000380860.3:n.2364+36dup
ENST00000422097.1:c.204+36dup	ENSP00000398776.1:n.204+36dup
ENST00000436117.2:c.2264+906dup	ENSP00000410980.2:n.2264+906dup
NM_000245.2:c.2364+36dup	NP_000236.2:n.2364+36dup
NM_001127500.1:c.2418+36dup , LRG_662t1:c.2418+36dup	NP_001120972.1:n.2418+36dup
XM_006715990.2:c.1074+36dup	XP_006716053.1:n.1074+36dup
XM_006715991.2:c.1074+36dup	XP_006716054.1:n.1074+36dup
XM_011516223.1:c.2421+36dup	XP_011514525.1:n.2421+36dup
NM_000245.3:c.2364+36dup	NP_000236.2:n.2364+36dup
NM_001127500.2:c.2418+36dup	NP_001120972.1:n.2418+36dup
NM_001324401.1:c.2364+36dup	NP_001311330.1:n.2364+36dup
NM_001324402.1:c.1074+36dup	NP_001311331.1:n.1074+36dup
XR_001744772.1:n.2495+906dup
NM_001127500.3:c.2418+36dup	NP_001120972.1:n.2418+36dup
NM_000245.4:c.2364+36dup MANE Select	NP_000236.2:n.2364+36dup
NM_001324401.2:c.2364+36dup	NP_001311330.1:n.2364+36dup
NM_001324402.2:c.1074+36dup	NP_001311331.1:n.1074+36dup
NM_001324401.3:c.2364+36dup	NP_001311330.1:n.2364+36dup