Canonical Allele Identifier: CA349991792
Gene: MSTN HGNC NCBI
C2orf88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190060393A>C , CM000664.2:g.190060393A>C GRCh38
NC_000002.11:g.190925119A>C , CM000664.1:g.190925119A>C GRCh37
NC_000002.10:g.190633364A>C NCBI36
NG_009800.1:g.7337T>G , LRG_200:g.7337T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260950.5:c.416T>G (MSTN) MANE Select ENSP00000260950.3:p.Phe139Cys
ENST00000260950.4:c.416T>G (MSTN) ENSP00000260950.3:p.Phe139Cys
ENST00000478197.1:n.220-18830A>C (C2orf88)
ENST00000495546.1:n.202-19561A>C (C2orf88)
NM_005259.2:c.416T>G , LRG_200t1:c.416T>G (MSTN) NP_005250.1:p.Phe139Cys
XM_005246905.1:c.-359-19561A>C (C2orf88) XP_005246962.1:n.-359-19561A>C
XM_011510958.1:c.32T>G (MSTN) XP_011509260.1:p.Phe11Cys
XM_011511982.1:c.-433-19561A>C (C2orf88) XP_011510284.1:n.-433-19561A>C
XM_011511986.1:c.-234-19561A>C (C2orf88) XP_011510288.1:n.-234-19561A>C
XM_011511986.2:c.-234-19561A>C (C2orf88) XP_011510288.1:n.-234-19561A>C
NM_005259.3:c.416T>G (MSTN) MANE Select NP_005250.1:p.Phe139Cys