Canonical Allele Identifier: CA2684591953

Gene: MET

Linked Data

• gnomAD v4: 7-116772090-AACCTAAAGGAAGTATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772095_116772111del , CM000669.2:g.116772095_116772111del	GRCh38
NC_000007.13:g.116412149_116412165del , CM000669.1:g.116412149_116412165del	GRCh37
NC_000007.12:g.116199385_116199401del	NCBI36
NG_008996.1:g.104691_104707del , LRG_662:g.104691_104707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+106_*633+122del	ENSP00000410980.2:n.*633+106_*633+122del
ENST00000318493.11:c.3082+106_3082+122del	ENSP00000317272.6:n.3082+106_3082+122del
ENST00000397752.8:c.3028+106_3028+122del MANE Select	ENSP00000380860.3:n.3028+106_3028+122del
ENST00000318493.10:c.3082+106_3082+122del	ENSP00000317272.6:n.3082+106_3082+122del
ENST00000397752.7:c.3028+106_3028+122del	ENSP00000380860.3:n.3028+106_3028+122del
ENST00000454623.1:c.283+441_283+457del	ENSP00000398140.1:n.283+441_283+457del
NM_000245.2:c.3028+106_3028+122del	NP_000236.2:n.3028+106_3028+122del
NM_001127500.1:c.3082+106_3082+122del , LRG_662t1:c.3082+106_3082+122del	NP_001120972.1:n.3082+106_3082+122del
XM_006715990.2:c.1738+106_1738+122del	XP_006716053.1:n.1738+106_1738+122del
XM_006715991.2:c.1738+106_1738+122del	XP_006716054.1:n.1738+106_1738+122del
XM_011516223.1:c.3085+106_3085+122del	XP_011514525.1:n.3085+106_3085+122del
NM_000245.3:c.3028+106_3028+122del	NP_000236.2:n.3028+106_3028+122del
NM_001127500.2:c.3082+106_3082+122del	NP_001120972.1:n.3082+106_3082+122del
NM_001324402.1:c.1738+106_1738+122del	NP_001311331.1:n.1738+106_1738+122del
XR_001744772.1:n.3159+106_3159+122del
NM_001127500.3:c.3082+106_3082+122del	NP_001120972.1:n.3082+106_3082+122del
NM_000245.4:c.3028+106_3028+122del MANE Select	NP_000236.2:n.3028+106_3028+122del
NM_001324402.2:c.1738+106_1738+122del	NP_001311331.1:n.1738+106_1738+122del