Canonical Allele Identifier: CA1315870345
Gene: MSTN HGNC NCBI
C2orf88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190058686A>T , CM000664.2:g.190058686A>T GRCh38
NC_000002.11:g.190923412A>T , CM000664.1:g.190923412A>T GRCh37
NC_000002.10:g.190631657A>T NCBI36
NG_009800.1:g.9044T>A , LRG_200:g.9044T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260950.5:c.748-1048T>A (MSTN) MANE Select ENSP00000260950.3:n.748-1048T>A
ENST00000260950.4:c.748-1048T>A (MSTN) ENSP00000260950.3:n.748-1048T>A
ENST00000478197.1:n.220-20537A>T (C2orf88)
ENST00000495546.1:n.202-21268A>T (C2orf88)
NM_005259.2:c.748-1048T>A , LRG_200t1:c.748-1048T>A (MSTN) NP_005250.1:n.748-1048T>A
XM_005246905.1:c.-359-21268A>T (C2orf88) XP_005246962.1:n.-359-21268A>T
XM_011510958.1:c.364-1048T>A (MSTN) XP_011509260.1:n.364-1048T>A
XM_011511982.1:c.-433-21268A>T (C2orf88) XP_011510284.1:n.-433-21268A>T
XM_011511986.1:c.-234-21268A>T (C2orf88) XP_011510288.1:n.-234-21268A>T
XM_011511986.2:c.-234-21268A>T (C2orf88) XP_011510288.1:n.-234-21268A>T
NM_005259.3:c.748-1048T>A (MSTN) MANE Select NP_005250.1:n.748-1048T>A
Search 100 bp 5'
Search 100 bp 3'