Canonical Allele Identifier: CA10612241

Gene: MSTN C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190056185C>A , CM000664.2:g.190056185C>A	GRCh38
NC_000002.11:g.190920911C>A , CM000664.1:g.190920911C>A	GRCh37
NC_000002.10:g.190629156C>A	NCBI36
NG_009800.1:g.11545G>T , LRG_200:g.11545G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005259.3:c.*1073G>T (MSTN) MANE Select	NP_005250.1:n.*1073G>T
ENST00000260950.5:c.*1073G>T (MSTN) MANE Select	ENSP00000260950.3:n.*1073G>T
NM_005259.2:c.*1073G>T , LRG_200t1:c.*1073G>T (MSTN)	NP_005250.1:n.*1073G>T
ENST00000260950.4:c.*1073G>T (MSTN)	ENSP00000260950.3:n.*1073G>T
ENST00000478197.1:n.220-23038C>A (C2orf88)
ENST00000495546.1:n.202-23769C>A (C2orf88)
XM_005246905.1:c.-359-23769C>A (C2orf88)	XP_005246962.1:n.-359-23769C>A
XM_011510958.1:c.*1073G>T (MSTN)	XP_011509260.1:n.*1073G>T
XM_011511982.1:c.-433-23769C>A (C2orf88)	XP_011510284.1:n.-433-23769C>A
XM_011511986.1:c.-234-23769C>A (C2orf88)	XP_011510288.1:n.-234-23769C>A
XM_011511986.2:c.-234-23769C>A (C2orf88)	XP_011510288.1:n.-234-23769C>A