Canonical Allele Identifier: CA1315870942

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060043A= , CM000664.2:g.190060043A=	GRCh38
NC_000002.11:g.190924769A= , CM000664.1:g.190924769A=	GRCh37
NC_000002.10:g.190633014A=	NCBI36
NG_009800.1:g.7687T= , LRG_200:g.7687T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.747+19T= (MSTN) MANE Select	ENSP00000260950.3:n.747+19T=
ENST00000260950.4:c.747+19T= (MSTN)	ENSP00000260950.3:n.747+19T=
ENST00000478197.1:n.220-19180A= (C2orf88)
ENST00000495546.1:n.202-19911A= (C2orf88)
NM_005259.2:c.747+19T= , LRG_200t1:c.747+19T= (MSTN)	NP_005250.1:n.747+19T=
XM_005246905.1:c.-359-19911A= (C2orf88)	XP_005246962.1:n.-359-19911A=
XM_011510958.1:c.363+19T= (MSTN)	XP_011509260.1:n.363+19T=
XM_011511982.1:c.-433-19911A= (C2orf88)	XP_011510284.1:n.-433-19911A=
XM_011511986.1:c.-234-19911A= (C2orf88)	XP_011510288.1:n.-234-19911A=
XM_011511986.2:c.-234-19911A= (C2orf88)	XP_011510288.1:n.-234-19911A=
NM_005259.3:c.747+19T= (MSTN) MANE Select	NP_005250.1:n.747+19T=