Canonical Allele Identifier: CA891841999

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771833_116771852del , CM000669.2:g.116771833_116771852del	GRCh38
NC_000007.13:g.116411887_116411906del , CM000669.1:g.116411887_116411906del	GRCh37
NC_000007.12:g.116199123_116199142del	NCBI36
NG_008996.1:g.104429_104448del , LRG_662:g.104429_104448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-16_*496del
ENST00000318493.11:c.2942-16_2945del
ENST00000397752.8:c.2888-16_2891del
ENST00000318493.10:c.2942-16_2945del
ENST00000397752.7:c.2888-16_2891del
ENST00000454623.1:c.283+179_283+198del	ENSP00000398140.1:n.283+179_283+198del
NM_000245.2:c.2888-16_2891del
NM_001127500.1:c.2942-16_2945del , LRG_662t1:c.2942-16_2945del
XM_006715990.2:c.1598-16_1601del
XM_006715991.2:c.1598-16_1601del
XM_011516223.1:c.2945-16_2948del
NM_000245.3:c.2888-16_2891del
NM_001127500.2:c.2942-16_2945del
NM_001324402.1:c.1598-16_1601del
XR_001744772.1:n.3019-16_3022del
NM_001127500.3:c.2942-16_2945del
NM_000245.4:c.2888-16_2891del
NM_001324402.2:c.1598-16_1601del