Canonical Allele Identifier: CA16612145

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116755465_116755467del , CM000669.2:g.116755465_116755467del	GRCh38
NC_000007.13:g.116395519_116395521del , CM000669.1:g.116395519_116395521del	GRCh37
NC_000007.12:g.116182755_116182757del	NCBI36
NG_008996.1:g.88061_88063del , LRG_662:g.88061_88063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1812_1814del	ENSP00000398776.2:p.Leu605del
ENST00000436117.3:c.1812_1814del	ENSP00000410980.2:p.Leu605del
ENST00000318493.11:c.1812_1814del	ENSP00000317272.6:p.Leu605del
ENST00000397752.8:c.1812_1814del MANE Select	ENSP00000380860.3:p.Leu605del
ENST00000318493.10:c.1812_1814del	ENSP00000317272.6:p.Leu605del
ENST00000397752.7:c.1812_1814del	ENSP00000380860.3:p.Leu605del
ENST00000436117.2:c.1812_1814del	ENSP00000410980.2:p.Leu605del
NM_000245.2:c.1812_1814del	NP_000236.2:p.Leu605del
NM_001127500.1:c.1812_1814del , LRG_662t1:c.1812_1814del	NP_001120972.1:p.Leu605del
XM_006715990.2:c.522_524del	XP_006716053.1:p.Leu175del
XM_006715991.2:c.522_524del	XP_006716054.1:p.Leu175del
XM_011516223.1:c.1869_1871del	XP_011514525.1:p.Leu624del
NM_000245.3:c.1812_1814del	NP_000236.2:p.Leu605del
NM_001127500.2:c.1812_1814del	NP_001120972.1:p.Leu605del
NM_001324401.1:c.1812_1814del	NP_001311330.1:p.Leu605del
NM_001324402.1:c.522_524del	NP_001311331.1:p.Leu175del
XR_001744772.1:n.2043_2045del
NM_001127500.3:c.1812_1814del	NP_001120972.1:p.Leu605del
NM_000245.4:c.1812_1814del MANE Select	NP_000236.2:p.Leu605del
NM_001324401.2:c.1812_1814del	NP_001311330.1:p.Leu605del
NM_001324402.2:c.522_524del	NP_001311331.1:p.Leu175del
NM_001324401.3:c.1812_1814del	NP_001311330.1:p.Leu605del