Canonical Allele Identifier: CA2662348949

Gene: MSTN C2orf88

Linked Data

• gnomAD v4: 2-190059958-AGCTTATGAGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190059959_190059969del , CM000664.2:g.190059959_190059969del	GRCh38
NC_000002.11:g.190924685_190924695del , CM000664.1:g.190924685_190924695del	GRCh37
NC_000002.10:g.190632930_190632940del	NCBI36
NG_009800.1:g.7761_7771del , LRG_200:g.7761_7771del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.747+93_747+103del (MSTN) MANE Select	ENSP00000260950.3:n.747+93_747+103del
ENST00000260950.4:c.747+93_747+103del (MSTN)	ENSP00000260950.3:n.747+93_747+103del
ENST00000478197.1:n.220-19264_220-19254del (C2orf88)
ENST00000495546.1:n.202-19995_202-19985del (C2orf88)
NM_005259.2:c.747+93_747+103del , LRG_200t1:c.747+93_747+103del (MSTN)	NP_005250.1:n.747+93_747+103del
XM_005246905.1:c.-359-19995_-359-19985del (C2orf88)	XP_005246962.1:n.-359-19995_-359-19985del
XM_011510958.1:c.363+93_363+103del (MSTN)	XP_011509260.1:n.363+93_363+103del
XM_011511982.1:c.-433-19995_-433-19985del (C2orf88)	XP_011510284.1:n.-433-19995_-433-19985del
XM_011511986.1:c.-234-19995_-234-19985del (C2orf88)	XP_011510288.1:n.-234-19995_-234-19985del
XM_011511986.2:c.-234-19995_-234-19985del (C2orf88)	XP_011510288.1:n.-234-19995_-234-19985del
NM_005259.3:c.747+93_747+103del (MSTN) MANE Select	NP_005250.1:n.747+93_747+103del