Canonical Allele Identifier: CA762317933

Gene: MSTN C2orf88

Linked Data

• dbSNP Id: rs1274021561
• gnomAD v3: 2-190062134-T-A
• gnomAD v4: 2-190062134-T-A
• MyVariant Identifiers: chr2:g.190926860T>A (hg19) ; chr2:g.190062134T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190062134T>A , CM000664.2:g.190062134T>A	GRCh38
NC_000002.11:g.190926860T>A , CM000664.1:g.190926860T>A	GRCh37
NC_000002.10:g.190635105T>A	NCBI36
NG_009800.1:g.5596A>T , LRG_200:g.5596A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260950.5:c.373+90A>T (MSTN) MANE Select	ENSP00000260950.3:n.373+90A>T
ENST00000260950.4:c.373+90A>T (MSTN)	ENSP00000260950.3:n.373+90A>T
ENST00000478197.1:n.220-17089T>A (C2orf88)
ENST00000495546.1:n.202-17820T>A (C2orf88)
NM_005259.2:c.373+90A>T , LRG_200t1:c.373+90A>T (MSTN)	NP_005250.1:n.373+90A>T
XM_005246905.1:c.-359-17820T>A (C2orf88)	XP_005246962.1:n.-359-17820T>A
XM_011511982.1:c.-433-17820T>A (C2orf88)	XP_011510284.1:n.-433-17820T>A
XM_011511986.1:c.-234-17820T>A (C2orf88)	XP_011510288.1:n.-234-17820T>A
XM_011511986.2:c.-234-17820T>A (C2orf88)	XP_011510288.1:n.-234-17820T>A
NM_005259.3:c.373+90A>T (MSTN) MANE Select	NP_005250.1:n.373+90A>T