Canonical Allele Identifier: CA1315871041

Gene: MSTN C2orf88

Linked Data

• dbSNP Id: rs1685556251

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060284_190060285insG , CM000664.2:g.190060284_190060285insG	GRCh38
NC_000002.11:g.190925010_190925011insG , CM000664.1:g.190925010_190925011insG	GRCh37
NC_000002.10:g.190633255_190633256insG	NCBI36
NG_009800.1:g.7445_7446insC , LRG_200:g.7445_7446insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.524_525insC (MSTN) MANE Select	ENSP00000260950.3:p.Arg175SerfsTer21
ENST00000260950.4:c.524_525insC (MSTN)	ENSP00000260950.3:p.Arg175SerfsTer21
ENST00000478197.1:n.220-18939_220-18938insG (C2orf88)
ENST00000495546.1:n.202-19670_202-19669insG (C2orf88)
NM_005259.2:c.524_525insC , LRG_200t1:c.524_525insC (MSTN)	NP_005250.1:p.Arg175SerfsTer21
XM_005246905.1:c.-359-19670_-359-19669insG (C2orf88)	XP_005246962.1:n.-359-19670_-359-19669insG
XM_011510958.1:c.140_141insC (MSTN)	XP_011509260.1:p.Arg47SerfsTer21
XM_011511982.1:c.-433-19670_-433-19669insG (C2orf88)	XP_011510284.1:n.-433-19670_-433-19669insG
XM_011511986.1:c.-234-19670_-234-19669insG (C2orf88)	XP_011510288.1:n.-234-19670_-234-19669insG
XM_011511986.2:c.-234-19670_-234-19669insG (C2orf88)	XP_011510288.1:n.-234-19670_-234-19669insG
NM_005259.3:c.524_525insC (MSTN) MANE Select	NP_005250.1:p.Arg175SerfsTer21