Canonical Allele Identifier: CA2715553389

Gene: MET

Linked Data

• dbSNP Id: rs2116997678

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771978_116771993del , CM000669.2:g.116771978_116771993del	GRCh38
NC_000007.13:g.116412032_116412047del , CM000669.1:g.116412032_116412047del	GRCh37
NC_000007.12:g.116199268_116199283del	NCBI36
NG_008996.1:g.104574_104589del , LRG_662:g.104574_104589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*622_*633+4del
ENST00000318493.11:c.3071_3082+4del
ENST00000397752.8:c.3017_3028+4del
ENST00000318493.10:c.3071_3082+4del
ENST00000397752.7:c.3017_3028+4del
ENST00000454623.1:c.283+324_283+339del	ENSP00000398140.1:n.283+324_283+339del
NM_000245.2:c.3017_3028+4del
NM_001127500.1:c.3071_3082+4del , LRG_662t1:c.3071_3082+4del
XM_006715990.2:c.1727_1738+4del
XM_006715991.2:c.1727_1738+4del
XM_011516223.1:c.3074_3085+4del
NM_000245.3:c.3017_3028+4del
NM_001127500.2:c.3071_3082+4del
NM_001324402.1:c.1727_1738+4del
XR_001744772.1:n.3148_3159+4del
NM_001127500.3:c.3071_3082+4del
NM_000245.4:c.3017_3028+4del
NM_001324402.2:c.1727_1738+4del