Canonical Allele Identifier: CA358275

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771972_116771998del , CM000669.2:g.116771972_116771998del	GRCh38
NC_000007.13:g.116412026_116412052del , CM000669.1:g.116412026_116412052del	GRCh37
NC_000007.12:g.116199262_116199288del	NCBI36
NG_008996.1:g.104568_104594del , LRG_662:g.104568_104594del

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.2:c.3011_3028+9del
NM_000245.3:c.3011_3028+9del
NM_000245.4:c.3011_3028+9del
NM_001127500.1:c.3065_3082+9del , LRG_662t1:c.3065_3082+9del
NM_001127500.2:c.3065_3082+9del
NM_001127500.3:c.3065_3082+9del
NM_001324402.1:c.1721_1738+9del
NM_001324402.2:c.1721_1738+9del
ENST00000318493.10:c.3065_3082+9del
ENST00000318493.11:c.3065_3082+9del
ENST00000397752.7:c.3011_3028+9del
ENST00000397752.8:c.3011_3028+9del
ENST00000436117.3:c.*616_*633+9del
ENST00000454623.1:c.283+318_283+344del	ENSP00000398140.1:n.283+318_283+344del
XM_006715990.2:c.1721_1738+9del
XM_006715991.2:c.1721_1738+9del
XM_011516223.1:c.3068_3085+9del
XR_001744772.1:n.3142_3159+9del