Canonical Allele Identifier: CA195544

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771592C>T , CM000669.2:g.116771592C>T	GRCh38
NC_000007.13:g.116411646C>T , CM000669.1:g.116411646C>T	GRCh37
NC_000007.12:g.116198882C>T	NCBI36
NG_008996.1:g.104188C>T , LRG_662:g.104188C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*430C>T	ENSP00000410980.2:n.*430C>T
ENST00000318493.11:c.2879C>T	ENSP00000317272.6:p.Ser960Leu
ENST00000397752.8:c.2825C>T MANE Select	ENSP00000380860.3:p.Ser942Leu
ENST00000318493.10:c.2879C>T	ENSP00000317272.6:p.Ser960Leu
ENST00000397752.7:c.2825C>T	ENSP00000380860.3:p.Ser942Leu
ENST00000454623.1:c.221C>T	ENSP00000398140.1:p.Ser74Leu
NM_000245.2:c.2825C>T	NP_000236.2:p.Ser942Leu
NM_001127500.1:c.2879C>T , LRG_662t1:c.2879C>T	NP_001120972.1:p.Ser960Leu
XM_006715990.2:c.1535C>T	XP_006716053.1:p.Ser512Leu
XM_006715991.2:c.1535C>T	XP_006716054.1:p.Ser512Leu
XM_011516223.1:c.2882C>T	XP_011514525.1:p.Ser961Leu
NM_000245.3:c.2825C>T	NP_000236.2:p.Ser942Leu
NM_001127500.2:c.2879C>T	NP_001120972.1:p.Ser960Leu
NM_001324402.1:c.1535C>T	NP_001311331.1:p.Ser512Leu
XR_001744772.1:n.2956C>T
NM_001127500.3:c.2879C>T	NP_001120972.1:p.Ser960Leu
NM_000245.4:c.2825C>T MANE Select	NP_000236.2:p.Ser942Leu
NM_001324402.2:c.1535C>T	NP_001311331.1:p.Ser512Leu