Canonical Allele Identifier: CA2662348934

Gene: MSTN C2orf88

Linked Data

• gnomAD v4: 2-190059932-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190059934del , CM000664.2:g.190059934del	GRCh38
NC_000002.11:g.190924660del , CM000664.1:g.190924660del	GRCh37
NC_000002.10:g.190632905del	NCBI36
NG_009800.1:g.7797del , LRG_200:g.7797del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.747+129del (MSTN) MANE Select	ENSP00000260950.3:n.747+129del
ENST00000260950.4:c.747+129del (MSTN)	ENSP00000260950.3:n.747+129del
ENST00000478197.1:n.220-19289del (C2orf88)
ENST00000495546.1:n.202-20020del (C2orf88)
NM_005259.2:c.747+129del , LRG_200t1:c.747+129del (MSTN)	NP_005250.1:n.747+129del
XM_005246905.1:c.-359-20020del (C2orf88)	XP_005246962.1:n.-359-20020del
XM_011510958.1:c.363+129del (MSTN)	XP_011509260.1:n.363+129del
XM_011511982.1:c.-433-20020del (C2orf88)	XP_011510284.1:n.-433-20020del
XM_011511986.1:c.-234-20020del (C2orf88)	XP_011510288.1:n.-234-20020del
XM_011511986.2:c.-234-20020del (C2orf88)	XP_011510288.1:n.-234-20020del
NM_005259.3:c.747+129del (MSTN) MANE Select	NP_005250.1:n.747+129del