Canonical Allele Identifier: CA1737014368

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783357T= , CM000669.2:g.116783357T=	GRCh38
NC_000007.13:g.116423411T= , CM000669.1:g.116423411T=	GRCh37
NC_000007.12:g.116210647T=	NCBI36
NG_008996.1:g.115953T= , LRG_662:g.115953T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1291T=	ENSP00000410980.2:n.*1291T=
ENST00000318493.11:c.3740T=	ENSP00000317272.6:p.Met1247=
ENST00000397752.8:c.3686T= MANE Select	ENSP00000380860.3:p.Met1229=
ENST00000318493.10:c.3740T=	ENSP00000317272.6:p.Met1247=
ENST00000397752.7:c.3686T=	ENSP00000380860.3:p.Met1229=
NM_000245.2:c.3686T=	NP_000236.2:p.Met1229=
NM_001127500.1:c.3740T= , LRG_662t1:c.3740T=	NP_001120972.1:p.Met1247=
XM_006715990.2:c.2396T=	XP_006716053.1:p.Met799=
XM_006715991.2:c.2396T=	XP_006716054.1:p.Met799=
XM_011516223.1:c.3743T=	XP_011514525.1:p.Met1248=
NM_000245.3:c.3686T=	NP_000236.2:p.Met1229=
NM_001127500.2:c.3740T=	NP_001120972.1:p.Met1247=
NM_001324402.1:c.2396T=	NP_001311331.1:p.Met799=
XR_001744772.1:n.3817T=
NM_001127500.3:c.3740T=	NP_001120972.1:p.Met1247=
NM_000245.4:c.3686T= MANE Select	NP_000236.2:p.Met1229=
NM_001324402.2:c.2396T=	NP_001311331.1:p.Met799=