Canonical Allele Identifier: CA1315870899

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190059937_190059938delinsTG , CM000664.2:g.190059937_190059938delinsTG	GRCh38
NC_000002.11:g.190924663_190924664delinsTG , CM000664.1:g.190924663_190924664delinsTG	GRCh37
NC_000002.10:g.190632908_190632909delinsTG	NCBI36
NG_009800.1:g.7792_7793delinsCA , LRG_200:g.7792_7793delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.747+124_747+125delinsCA (MSTN) MANE Select	ENSP00000260950.3:n.747+124_747+125delinsCA
ENST00000260950.4:c.747+124_747+125delinsCA (MSTN)	ENSP00000260950.3:n.747+124_747+125delinsCA
ENST00000478197.1:n.220-19286_220-19285delinsTG (C2orf88)
ENST00000495546.1:n.202-20017_202-20016delinsTG (C2orf88)
NM_005259.2:c.747+124_747+125delinsCA , LRG_200t1:c.747+124_747+125delinsCA (MSTN)	NP_005250.1:n.747+124_747+125delinsCA
XM_005246905.1:c.-359-20017_-359-20016delinsTG (C2orf88)	XP_005246962.1:n.-359-20017_-359-20016delinsTG
XM_011510958.1:c.363+124_363+125delinsCA (MSTN)	XP_011509260.1:n.363+124_363+125delinsCA
XM_011511982.1:c.-433-20017_-433-20016delinsTG (C2orf88)	XP_011510284.1:n.-433-20017_-433-20016delinsTG
XM_011511986.1:c.-234-20017_-234-20016delinsTG (C2orf88)	XP_011510288.1:n.-234-20017_-234-20016delinsTG
XM_011511986.2:c.-234-20017_-234-20016delinsTG (C2orf88)	XP_011510288.1:n.-234-20017_-234-20016delinsTG
NM_005259.3:c.747+124_747+125delinsCA (MSTN) MANE Select	NP_005250.1:n.747+124_747+125delinsCA