Canonical Allele Identifier: CA1737014360

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783356A= , CM000669.2:g.116783356A=	GRCh38
NC_000007.13:g.116423410A= , CM000669.1:g.116423410A=	GRCh37
NC_000007.12:g.116210646A=	NCBI36
NG_008996.1:g.115952A= , LRG_662:g.115952A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1290A=	ENSP00000410980.2:n.*1290A=
ENST00000318493.11:c.3739A=	ENSP00000317272.6:p.Met1247=
ENST00000397752.8:c.3685A= MANE Select	ENSP00000380860.3:p.Met1229=
ENST00000318493.10:c.3739A=	ENSP00000317272.6:p.Met1247=
ENST00000397752.7:c.3685A=	ENSP00000380860.3:p.Met1229=
NM_000245.2:c.3685A=	NP_000236.2:p.Met1229=
NM_001127500.1:c.3739A= , LRG_662t1:c.3739A=	NP_001120972.1:p.Met1247=
XM_006715990.2:c.2395A=	XP_006716053.1:p.Met799=
XM_006715991.2:c.2395A=	XP_006716054.1:p.Met799=
XM_011516223.1:c.3742A=	XP_011514525.1:p.Met1248=
NM_000245.3:c.3685A=	NP_000236.2:p.Met1229=
NM_001127500.2:c.3739A=	NP_001120972.1:p.Met1247=
NM_001324402.1:c.2395A=	NP_001311331.1:p.Met799=
XR_001744772.1:n.3816A=
NM_001127500.3:c.3739A=	NP_001120972.1:p.Met1247=
NM_000245.4:c.3685A= MANE Select	NP_000236.2:p.Met1229=
NM_001324402.2:c.2395A=	NP_001311331.1:p.Met799=