Canonical Allele Identifier: CA368982373

Gene: MET

Linked Data

• dbSNP Id: rs748086754
• MyVariant Identifiers: chr7:g.116399505G>C (hg19) ; chr7:g.116759451G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759451G>C , CM000669.2:g.116759451G>C	GRCh38
NC_000007.13:g.116399505G>C , CM000669.1:g.116399505G>C	GRCh37
NC_000007.12:g.116186741G>C	NCBI36
NG_008996.1:g.92047G>C , LRG_662:g.92047G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2325G>C	ENSP00000398776.2:p.Met775Ile
ENST00000436117.3:c.2264+831G>C	ENSP00000410980.2:n.2264+831G>C
ENST00000318493.11:c.2379G>C	ENSP00000317272.6:p.Met793Ile
ENST00000397752.8:c.2325G>C MANE Select	ENSP00000380860.3:p.Met775Ile
ENST00000318493.10:c.2379G>C	ENSP00000317272.6:p.Met793Ile
ENST00000397752.7:c.2325G>C	ENSP00000380860.3:p.Met775Ile
ENST00000422097.1:c.165G>C	ENSP00000398776.1:p.Met55Ile
ENST00000436117.2:c.2264+831G>C	ENSP00000410980.2:n.2264+831G>C
NM_000245.2:c.2325G>C	NP_000236.2:p.Met775Ile
NM_001127500.1:c.2379G>C , LRG_662t1:c.2379G>C	NP_001120972.1:p.Met793Ile
XM_006715990.2:c.1035G>C	XP_006716053.1:p.Met345Ile
XM_006715991.2:c.1035G>C	XP_006716054.1:p.Met345Ile
XM_011516223.1:c.2382G>C	XP_011514525.1:p.Met794Ile
NM_000245.3:c.2325G>C	NP_000236.2:p.Met775Ile
NM_001127500.2:c.2379G>C	NP_001120972.1:p.Met793Ile
NM_001324401.1:c.2325G>C	NP_001311330.1:p.Met775Ile
NM_001324402.1:c.1035G>C	NP_001311331.1:p.Met345Ile
XR_001744772.1:n.2495+831G>C
NM_001127500.3:c.2379G>C	NP_001120972.1:p.Met793Ile
NM_000245.4:c.2325G>C MANE Select	NP_000236.2:p.Met775Ile
NM_001324401.2:c.2325G>C	NP_001311330.1:p.Met775Ile
NM_001324402.2:c.1035G>C	NP_001311331.1:p.Met345Ile
NM_001324401.3:c.2325G>C	NP_001311330.1:p.Met775Ile