Canonical Allele Identifier: CA1315870933

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060034_190060037delinsTATA , CM000664.2:g.190060034_190060037delinsTATA	GRCh38
NC_000002.11:g.190924760_190924763delinsTATA , CM000664.1:g.190924760_190924763delinsTATA	GRCh37
NC_000002.10:g.190633005_190633008delinsTATA	NCBI36
NG_009800.1:g.7693_7696delinsTATA , LRG_200:g.7693_7696delinsTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.747+25_747+28delinsTATA (MSTN) MANE Select	ENSP00000260950.3:n.747+25_747+28delinsTATA
ENST00000260950.4:c.747+25_747+28delinsTATA (MSTN)	ENSP00000260950.3:n.747+25_747+28delinsTATA
ENST00000478197.1:n.220-19189_220-19186delinsTATA (C2orf88)
ENST00000495546.1:n.202-19920_202-19917delinsTATA (C2orf88)
NM_005259.2:c.747+25_747+28delinsTATA , LRG_200t1:c.747+25_747+28delinsTATA (MSTN)	NP_005250.1:n.747+25_747+28delinsTATA
XM_005246905.1:c.-359-19920_-359-19917delinsTATA (C2orf88)	XP_005246962.1:n.-359-19920_-359-19917delinsTATA
XM_011510958.1:c.363+25_363+28delinsTATA (MSTN)	XP_011509260.1:n.363+25_363+28delinsTATA
XM_011511982.1:c.-433-19920_-433-19917delinsTATA (C2orf88)	XP_011510284.1:n.-433-19920_-433-19917delinsTATA
XM_011511986.1:c.-234-19920_-234-19917delinsTATA (C2orf88)	XP_011510288.1:n.-234-19920_-234-19917delinsTATA
XM_011511986.2:c.-234-19920_-234-19917delinsTATA (C2orf88)	XP_011510288.1:n.-234-19920_-234-19917delinsTATA
NM_005259.3:c.747+25_747+28delinsTATA (MSTN) MANE Select	NP_005250.1:n.747+25_747+28delinsTATA