Canonical Allele Identifier: CA2662349002

Gene: MSTN C2orf88

Linked Data

• gnomAD v4: 2-190060329-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060331_190060332dup , CM000664.2:g.190060331_190060332dup	GRCh38
NC_000002.11:g.190925057_190925058dup , CM000664.1:g.190925057_190925058dup	GRCh37
NC_000002.10:g.190633302_190633303dup	NCBI36
NG_009800.1:g.7399_7400dup , LRG_200:g.7399_7400dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.478_479dup (MSTN) MANE Select	ENSP00000260950.3:p.Leu160PhefsTer2
ENST00000260950.4:c.478_479dup (MSTN)	ENSP00000260950.3:p.Leu160PhefsTer2
ENST00000478197.1:n.220-18892_220-18891dup (C2orf88)
ENST00000495546.1:n.202-19623_202-19622dup (C2orf88)
NM_005259.2:c.478_479dup , LRG_200t1:c.478_479dup (MSTN)	NP_005250.1:p.Leu160PhefsTer2
XM_005246905.1:c.-359-19623_-359-19622dup (C2orf88)	XP_005246962.1:n.-359-19623_-359-19622dup
XM_011510958.1:c.94_95dup (MSTN)	XP_011509260.1:p.Leu32PhefsTer2
XM_011511982.1:c.-433-19623_-433-19622dup (C2orf88)	XP_011510284.1:n.-433-19623_-433-19622dup
XM_011511986.1:c.-234-19623_-234-19622dup (C2orf88)	XP_011510288.1:n.-234-19623_-234-19622dup
XM_011511986.2:c.-234-19623_-234-19622dup (C2orf88)	XP_011510288.1:n.-234-19623_-234-19622dup
NM_005259.3:c.478_479dup (MSTN) MANE Select	NP_005250.1:p.Leu160PhefsTer2