Canonical Allele Identifier: CA2027015

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190057324A>G , CM000664.2:g.190057324A>G	GRCh38
NC_000002.11:g.190922050A>G , CM000664.1:g.190922050A>G	GRCh37
NC_000002.10:g.190630295A>G	NCBI36
NG_009800.1:g.10406T>C , LRG_200:g.10406T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005259.3:c.1062T>C (MSTN) MANE Select	NP_005250.1:p.Asn354=
ENST00000260950.5:c.1062T>C (MSTN) MANE Select	ENSP00000260950.3:p.Asn354=
NM_005259.2:c.1062T>C , LRG_200t1:c.1062T>C (MSTN)	NP_005250.1:p.Asn354=
ENST00000260950.4:c.1062T>C (MSTN)	ENSP00000260950.3:p.Asn354=
ENST00000478197.1:n.220-21899A>G (C2orf88)
ENST00000495546.1:n.202-22630A>G (C2orf88)
XM_005246905.1:c.-359-22630A>G (C2orf88)	XP_005246962.1:n.-359-22630A>G
XM_011510958.1:c.678T>C (MSTN)	XP_011509260.1:p.Asn226=
XM_011511982.1:c.-433-22630A>G (C2orf88)	XP_011510284.1:n.-433-22630A>G
XM_011511986.1:c.-234-22630A>G (C2orf88)	XP_011510288.1:n.-234-22630A>G
XM_011511986.2:c.-234-22630A>G (C2orf88)	XP_011510288.1:n.-234-22630A>G