Canonical Allele Identifier: CA2662349001

Gene: MSTN C2orf88

Linked Data

• gnomAD v4: 2-190060304-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060306_190060307del , CM000664.2:g.190060306_190060307del	GRCh38
NC_000002.11:g.190925032_190925033del , CM000664.1:g.190925032_190925033del	GRCh37
NC_000002.10:g.190633277_190633278del	NCBI36
NG_009800.1:g.7424_7425del , LRG_200:g.7424_7425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.503_504del (MSTN) MANE Select	ENSP00000260950.3:p.Thr168SerfsTer27
ENST00000260950.4:c.503_504del (MSTN)	ENSP00000260950.3:p.Thr168SerfsTer27
ENST00000478197.1:n.220-18917_220-18916del (C2orf88)
ENST00000495546.1:n.202-19648_202-19647del (C2orf88)
NM_005259.2:c.503_504del , LRG_200t1:c.503_504del (MSTN)	NP_005250.1:p.Thr168SerfsTer27
XM_005246905.1:c.-359-19648_-359-19647del (C2orf88)	XP_005246962.1:n.-359-19648_-359-19647del
XM_011510958.1:c.119_120del (MSTN)	XP_011509260.1:p.Thr40SerfsTer27
XM_011511982.1:c.-433-19648_-433-19647del (C2orf88)	XP_011510284.1:n.-433-19648_-433-19647del
XM_011511986.1:c.-234-19648_-234-19647del (C2orf88)	XP_011510288.1:n.-234-19648_-234-19647del
XM_011511986.2:c.-234-19648_-234-19647del (C2orf88)	XP_011510288.1:n.-234-19648_-234-19647del
NM_005259.3:c.503_504del (MSTN) MANE Select	NP_005250.1:p.Thr168SerfsTer27