Canonical Allele Identifier: CA2555631232

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772180_116772184del , CM000669.2:g.116772180_116772184del	GRCh38
NC_000007.13:g.116412234_116412238del , CM000669.1:g.116412234_116412238del	GRCh37
NC_000007.12:g.116199470_116199474del	NCBI36
NG_008996.1:g.104776_104780del , LRG_662:g.104776_104780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+191_*633+195del	ENSP00000410980.2:n.*633+191_*633+195del
ENST00000318493.11:c.3082+191_3082+195del	ENSP00000317272.6:n.3082+191_3082+195del
ENST00000397752.8:c.3028+191_3028+195del MANE Select	ENSP00000380860.3:n.3028+191_3028+195del
ENST00000318493.10:c.3082+191_3082+195del	ENSP00000317272.6:n.3082+191_3082+195del
ENST00000397752.7:c.3028+191_3028+195del	ENSP00000380860.3:n.3028+191_3028+195del
ENST00000454623.1:c.283+526_283+530del	ENSP00000398140.1:n.283+526_283+530del
NM_000245.2:c.3028+191_3028+195del	NP_000236.2:n.3028+191_3028+195del
NM_001127500.1:c.3082+191_3082+195del , LRG_662t1:c.3082+191_3082+195del	NP_001120972.1:n.3082+191_3082+195del
XM_006715990.2:c.1738+191_1738+195del	XP_006716053.1:n.1738+191_1738+195del
XM_006715991.2:c.1738+191_1738+195del	XP_006716054.1:n.1738+191_1738+195del
XM_011516223.1:c.3085+191_3085+195del	XP_011514525.1:n.3085+191_3085+195del
NM_000245.3:c.3028+191_3028+195del	NP_000236.2:n.3028+191_3028+195del
NM_001127500.2:c.3082+191_3082+195del	NP_001120972.1:n.3082+191_3082+195del
NM_001324402.1:c.1738+191_1738+195del	NP_001311331.1:n.1738+191_1738+195del
XR_001744772.1:n.3159+191_3159+195del
NM_001127500.3:c.3082+191_3082+195del	NP_001120972.1:n.3082+191_3082+195del
NM_000245.4:c.3028+191_3028+195del MANE Select	NP_000236.2:n.3028+191_3028+195del
NM_001324402.2:c.1738+191_1738+195del	NP_001311331.1:n.1738+191_1738+195del