Canonical Allele Identifier: CA762316315

Gene: MSTN C2orf88

Linked Data

• dbSNP Id: rs1295174237
• MyVariant Identifiers: chr2:g.190924664del (hg19) ; chr2:g.190059938del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190059941del , CM000664.2:g.190059941del	GRCh38
NC_000002.11:g.190924667del , CM000664.1:g.190924667del	GRCh37
NC_000002.10:g.190632912del	NCBI36
NG_009800.1:g.7792del , LRG_200:g.7792del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.747+124del (MSTN) MANE Select	ENSP00000260950.3:n.747+124del
ENST00000260950.4:c.747+124del (MSTN)	ENSP00000260950.3:n.747+124del
ENST00000478197.1:n.220-19282del (C2orf88)
ENST00000495546.1:n.202-20013del (C2orf88)
NM_005259.2:c.747+124del , LRG_200t1:c.747+124del (MSTN)	NP_005250.1:n.747+124del
XM_005246905.1:c.-359-20013del (C2orf88)	XP_005246962.1:n.-359-20013del
XM_011510958.1:c.363+124del (MSTN)	XP_011509260.1:n.363+124del
XM_011511982.1:c.-433-20013del (C2orf88)	XP_011510284.1:n.-433-20013del
XM_011511986.1:c.-234-20013del (C2orf88)	XP_011510288.1:n.-234-20013del
XM_011511986.2:c.-234-20013del (C2orf88)	XP_011510288.1:n.-234-20013del
NM_005259.3:c.747+124del (MSTN) MANE Select	NP_005250.1:n.747+124del