Canonical Allele Identifier: CA349991628
Gene: MSTN HGNC NCBI
C2orf88 HGNC NCBI

Linked Data

dbSNP Id: rs1356908296

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190060322C>G , CM000664.2:g.190060322C>G GRCh38
NC_000002.11:g.190925048C>G , CM000664.1:g.190925048C>G GRCh37
NC_000002.10:g.190633293C>G NCBI36
NG_009800.1:g.7408G>C , LRG_200:g.7408G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260950.5:c.487G>C (MSTN) MANE Select ENSP00000260950.3:p.Val163Leu
ENST00000260950.4:c.487G>C (MSTN) ENSP00000260950.3:p.Val163Leu
ENST00000478197.1:n.220-18901C>G (C2orf88)
ENST00000495546.1:n.202-19632C>G (C2orf88)
NM_005259.2:c.487G>C , LRG_200t1:c.487G>C (MSTN) NP_005250.1:p.Val163Leu
XM_005246905.1:c.-359-19632C>G (C2orf88) XP_005246962.1:n.-359-19632C>G
XM_011510958.1:c.103G>C (MSTN) XP_011509260.1:p.Val35Leu
XM_011511982.1:c.-433-19632C>G (C2orf88) XP_011510284.1:n.-433-19632C>G
XM_011511986.1:c.-234-19632C>G (C2orf88) XP_011510288.1:n.-234-19632C>G
XM_011511986.2:c.-234-19632C>G (C2orf88) XP_011510288.1:n.-234-19632C>G
NM_005259.3:c.487G>C (MSTN) MANE Select NP_005250.1:p.Val163Leu