Canonical Allele Identifier: CA2201238956

Gene: MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.768807C= , CM000678.2:g.768807C=	GRCh38
NC_000016.9:g.818807C= , CM000678.1:g.818807C=	GRCh37
NC_000016.8:g.758808C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005823.6:c.*74C= MANE Select	NP_005814.2:n.*74C=
ENST00000545450.7:c.*74C= MANE Select	ENSP00000442965.2:n.*74C=
NM_001177355.1:c.*74C=	NP_001170826.1:n.*74C=
NM_001177355.2:c.*74C=	NP_001170826.1:n.*74C=
NM_001177355.3:c.*74C=	NP_001170826.1:n.*74C=
NM_005823.5:c.*74C=	NP_005814.2:n.*74C=
NM_013404.4:c.*74C=	NP_037536.2:n.*74C=
ENST00000382862.7:c.*74C=	ENSP00000372313.3:n.*74C=
ENST00000545450.6:c.*74C=	ENSP00000442965.2:n.*74C=
ENST00000561896.1:c.1137C=	ENSP00000457847.1:p.Pro379=
ENST00000563941.5:c.*74C=	ENSP00000456008.1:n.*74C=
ENST00000566549.5:c.*74C=	ENSP00000456702.1:n.*74C=
ENST00000620831.4:c.*74C=	ENSP00000482893.1:n.*74C=
XM_005255034.3:c.*74C=	XP_005255091.1:n.*74C=
XM_006720837.2:c.*74C=	XP_006720900.1:n.*74C=
XM_011522346.1:c.*74C=	XP_011520648.1:n.*74C=
XM_011522347.1:c.*74C=	XP_011520649.1:n.*74C=
XM_011522348.1:c.*74C=	XP_011520650.1:n.*74C=
XM_011522349.1:c.*74C=	XP_011520651.1:n.*74C=
XM_011522350.1:c.*74C=	XP_011520652.1:n.*74C=