Canonical Allele Identifier: CA2662349125

Gene: MSTN C2orf88

Linked Data

• gnomAD v4: 2-190062123-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190062123C>A , CM000664.2:g.190062123C>A	GRCh38
NC_000002.11:g.190926849C>A , CM000664.1:g.190926849C>A	GRCh37
NC_000002.10:g.190635094C>A	NCBI36
NG_009800.1:g.5607G>T , LRG_200:g.5607G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260950.5:c.373+101G>T (MSTN) MANE Select	ENSP00000260950.3:n.373+101G>T
ENST00000260950.4:c.373+101G>T (MSTN)	ENSP00000260950.3:n.373+101G>T
ENST00000478197.1:n.220-17100C>A (C2orf88)
ENST00000495546.1:n.202-17831C>A (C2orf88)
NM_005259.2:c.373+101G>T , LRG_200t1:c.373+101G>T (MSTN)	NP_005250.1:n.373+101G>T
XM_005246905.1:c.-359-17831C>A (C2orf88)	XP_005246962.1:n.-359-17831C>A
XM_011511982.1:c.-433-17831C>A (C2orf88)	XP_011510284.1:n.-433-17831C>A
XM_011511986.1:c.-234-17831C>A (C2orf88)	XP_011510288.1:n.-234-17831C>A
XM_011511986.2:c.-234-17831C>A (C2orf88)	XP_011510288.1:n.-234-17831C>A
NM_005259.3:c.373+101G>T (MSTN) MANE Select	NP_005250.1:n.373+101G>T