Canonical Allele Identifier: CA2832529140

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771890_116772201del , CM000669.2:g.116771890_116772201del	GRCh38
NC_000007.13:g.116411944_116412255del , CM000669.1:g.116411944_116412255del	GRCh37
NC_000007.12:g.116199180_116199491del	NCBI36
NG_008996.1:g.104486_104797del , LRG_662:g.104486_104797del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*534_*633+212del
ENST00000318493.11:c.2983_3082+212del
ENST00000397752.8:c.2929_3028+212del
ENST00000318493.10:c.2983_3082+212del
ENST00000397752.7:c.2929_3028+212del
ENST00000454623.1:c.283+236_283+547del	ENSP00000398140.1:n.283+236_283+547del
NM_000245.2:c.2929_3028+212del
NM_001127500.1:c.2983_3082+212del , LRG_662t1:c.2983_3082+212del
XM_006715990.2:c.1639_1738+212del
XM_006715991.2:c.1639_1738+212del
XM_011516223.1:c.2986_3085+212del
NM_000245.3:c.2929_3028+212del
NM_001127500.2:c.2983_3082+212del
NM_001324402.1:c.1639_1738+212del
XR_001744772.1:n.3060_3159+212del
NM_001127500.3:c.2983_3082+212del
NM_000245.4:c.2929_3028+212del
NM_001324402.2:c.1639_1738+212del