Canonical Allele Identifier: CA2027226

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190062613T>G , CM000664.2:g.190062613T>G	GRCh38
NC_000002.11:g.190927339T>G , CM000664.1:g.190927339T>G	GRCh37
NC_000002.10:g.190635584T>G	NCBI36
NG_009800.1:g.5117A>C , LRG_200:g.5117A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005259.3:c.-17A>C (MSTN) MANE Select	NP_005250.1:n.-17A>C
ENST00000260950.5:c.-17A>C (MSTN) MANE Select	ENSP00000260950.3:n.-17A>C
NM_005259.2:c.-17A>C , LRG_200t1:c.-17A>C (MSTN)	NP_005250.1:n.-17A>C
ENST00000260950.4:c.-17A>C (MSTN)	ENSP00000260950.3:n.-17A>C
ENST00000478197.1:n.220-16610T>G (C2orf88)
ENST00000495546.1:n.202-17341T>G (C2orf88)
XM_005246905.1:c.-359-17341T>G (C2orf88)	XP_005246962.1:n.-359-17341T>G
XM_011511982.1:c.-433-17341T>G (C2orf88)	XP_011510284.1:n.-433-17341T>G
XM_011511986.1:c.-234-17341T>G (C2orf88)	XP_011510288.1:n.-234-17341T>G
XM_011511986.2:c.-234-17341T>G (C2orf88)	XP_011510288.1:n.-234-17341T>G