Canonical Allele Identifier: CA2027229

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190062638_190062640del , CM000664.2:g.190062638_190062640del	GRCh38
NC_000002.11:g.190927364_190927366del , CM000664.1:g.190927364_190927366del	GRCh37
NC_000002.10:g.190635609_190635611del	NCBI36
NG_009800.1:g.5093_5095del , LRG_200:g.5093_5095del

Transcript Alleles

HGVS	Amino-acid Change
NM_005259.3:c.-41_-39del (MSTN) MANE Select	NP_005250.1:n.-41_-39del
ENST00000260950.5:c.-41_-39del (MSTN) MANE Select	ENSP00000260950.3:n.-41_-39del
NM_005259.2:c.-41_-39del , LRG_200t1:c.-41_-39del (MSTN)	NP_005250.1:n.-41_-39del
ENST00000260950.4:c.-41_-39del (MSTN)	ENSP00000260950.3:n.-41_-39del
ENST00000478197.1:n.220-16585_220-16583del (C2orf88)
ENST00000495546.1:n.202-17316_202-17314del (C2orf88)
XM_005246905.1:c.-359-17316_-359-17314del (C2orf88)	XP_005246962.1:n.-359-17316_-359-17314del
XM_011511982.1:c.-433-17316_-433-17314del (C2orf88)	XP_011510284.1:n.-433-17316_-433-17314del
XM_011511986.1:c.-234-17316_-234-17314del (C2orf88)	XP_011510288.1:n.-234-17316_-234-17314del
XM_011511986.2:c.-234-17316_-234-17314del (C2orf88)	XP_011510288.1:n.-234-17316_-234-17314del