Canonical Allele Identifier: CA2684591939

Gene: MET

Linked Data

• gnomAD v4: 7-116772052-GTTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772055_116772058del , CM000669.2:g.116772055_116772058del	GRCh38
NC_000007.13:g.116412109_116412112del , CM000669.1:g.116412109_116412112del	GRCh37
NC_000007.12:g.116199345_116199348del	NCBI36
NG_008996.1:g.104651_104654del , LRG_662:g.104651_104654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+66_*633+69del	ENSP00000410980.2:n.*633+66_*633+69del
ENST00000318493.11:c.3082+66_3082+69del	ENSP00000317272.6:n.3082+66_3082+69del
ENST00000397752.8:c.3028+66_3028+69del MANE Select	ENSP00000380860.3:n.3028+66_3028+69del
ENST00000318493.10:c.3082+66_3082+69del	ENSP00000317272.6:n.3082+66_3082+69del
ENST00000397752.7:c.3028+66_3028+69del	ENSP00000380860.3:n.3028+66_3028+69del
ENST00000454623.1:c.283+401_283+404del	ENSP00000398140.1:n.283+401_283+404del
NM_000245.2:c.3028+66_3028+69del	NP_000236.2:n.3028+66_3028+69del
NM_001127500.1:c.3082+66_3082+69del , LRG_662t1:c.3082+66_3082+69del	NP_001120972.1:n.3082+66_3082+69del
XM_006715990.2:c.1738+66_1738+69del	XP_006716053.1:n.1738+66_1738+69del
XM_006715991.2:c.1738+66_1738+69del	XP_006716054.1:n.1738+66_1738+69del
XM_011516223.1:c.3085+66_3085+69del	XP_011514525.1:n.3085+66_3085+69del
NM_000245.3:c.3028+66_3028+69del	NP_000236.2:n.3028+66_3028+69del
NM_001127500.2:c.3082+66_3082+69del	NP_001120972.1:n.3082+66_3082+69del
NM_001324402.1:c.1738+66_1738+69del	NP_001311331.1:n.1738+66_1738+69del
XR_001744772.1:n.3159+66_3159+69del
NM_001127500.3:c.3082+66_3082+69del	NP_001120972.1:n.3082+66_3082+69del
NM_000245.4:c.3028+66_3028+69del MANE Select	NP_000236.2:n.3028+66_3028+69del
NM_001324402.2:c.1738+66_1738+69del	NP_001311331.1:n.1738+66_1738+69del