Canonical Allele Identifier: CA368986813

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116411703T>C (hg19) ; chr7:g.116771649T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771649T>C , CM000669.2:g.116771649T>C	GRCh38
NC_000007.13:g.116411703T>C , CM000669.1:g.116411703T>C	GRCh37
NC_000007.12:g.116198939T>C	NCBI36
NG_008996.1:g.104245T>C , LRG_662:g.104245T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*487T>C	ENSP00000410980.2:n.*487T>C
ENST00000318493.11:c.2936T>C	ENSP00000317272.6:p.Ile979Thr
ENST00000397752.8:c.2882T>C MANE Select	ENSP00000380860.3:p.Ile961Thr
ENST00000318493.10:c.2936T>C	ENSP00000317272.6:p.Ile979Thr
ENST00000397752.7:c.2882T>C	ENSP00000380860.3:p.Ile961Thr
ENST00000454623.1:c.278T>C	ENSP00000398140.1:p.Ile93Thr
NM_000245.2:c.2882T>C	NP_000236.2:p.Ile961Thr
NM_001127500.1:c.2936T>C , LRG_662t1:c.2936T>C	NP_001120972.1:p.Ile979Thr
XM_006715990.2:c.1592T>C	XP_006716053.1:p.Ile531Thr
XM_006715991.2:c.1592T>C	XP_006716054.1:p.Ile531Thr
XM_011516223.1:c.2939T>C	XP_011514525.1:p.Ile980Thr
NM_000245.3:c.2882T>C	NP_000236.2:p.Ile961Thr
NM_001127500.2:c.2936T>C	NP_001120972.1:p.Ile979Thr
NM_001324402.1:c.1592T>C	NP_001311331.1:p.Ile531Thr
XR_001744772.1:n.3013T>C
NM_001127500.3:c.2936T>C	NP_001120972.1:p.Ile979Thr
NM_000245.4:c.2882T>C MANE Select	NP_000236.2:p.Ile961Thr
NM_001324402.2:c.1592T>C	NP_001311331.1:p.Ile531Thr