Canonical Allele Identifier: CA1315870921
Gene: MSTN HGNC NCBI
C2orf88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190060017_190060018delinsTA , CM000664.2:g.190060017_190060018delinsTA GRCh38
NC_000002.11:g.190924743_190924744delinsTA , CM000664.1:g.190924743_190924744delinsTA GRCh37
NC_000002.10:g.190632988_190632989delinsTA NCBI36
NG_009800.1:g.7712_7713delinsTA , LRG_200:g.7712_7713delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260950.5:c.747+44_747+45delinsTA (MSTN) MANE Select ENSP00000260950.3:n.747+44_747+45delinsTA
ENST00000260950.4:c.747+44_747+45delinsTA (MSTN) ENSP00000260950.3:n.747+44_747+45delinsTA
ENST00000478197.1:n.220-19206_220-19205delinsTA (C2orf88)
ENST00000495546.1:n.202-19937_202-19936delinsTA (C2orf88)
NM_005259.2:c.747+44_747+45delinsTA , LRG_200t1:c.747+44_747+45delinsTA (MSTN) NP_005250.1:n.747+44_747+45delinsTA
XM_005246905.1:c.-359-19937_-359-19936delinsTA (C2orf88) XP_005246962.1:n.-359-19937_-359-19936delinsTA
XM_011510958.1:c.363+44_363+45delinsTA (MSTN) XP_011509260.1:n.363+44_363+45delinsTA
XM_011511982.1:c.-433-19937_-433-19936delinsTA (C2orf88) XP_011510284.1:n.-433-19937_-433-19936delinsTA
XM_011511986.1:c.-234-19937_-234-19936delinsTA (C2orf88) XP_011510288.1:n.-234-19937_-234-19936delinsTA
XM_011511986.2:c.-234-19937_-234-19936delinsTA (C2orf88) XP_011510288.1:n.-234-19937_-234-19936delinsTA
NM_005259.3:c.747+44_747+45delinsTA (MSTN) MANE Select NP_005250.1:n.747+44_747+45delinsTA