Canonical Allele Identifier: CA349991771

Gene: MSTN C2orf88

Linked Data

• MyVariant Identifiers: chr2:g.190925111A>C (hg19) ; chr2:g.190060385A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060385A>C , CM000664.2:g.190060385A>C	GRCh38
NC_000002.11:g.190925111A>C , CM000664.1:g.190925111A>C	GRCh37
NC_000002.10:g.190633356A>C	NCBI36
NG_009800.1:g.7345T>G , LRG_200:g.7345T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.424T>G (MSTN) MANE Select	ENSP00000260950.3:p.Phe142Val
ENST00000260950.4:c.424T>G (MSTN)	ENSP00000260950.3:p.Phe142Val
ENST00000478197.1:n.220-18838A>C (C2orf88)
ENST00000495546.1:n.202-19569A>C (C2orf88)
NM_005259.2:c.424T>G , LRG_200t1:c.424T>G (MSTN)	NP_005250.1:p.Phe142Val
XM_005246905.1:c.-359-19569A>C (C2orf88)	XP_005246962.1:n.-359-19569A>C
XM_011510958.1:c.40T>G (MSTN)	XP_011509260.1:p.Phe14Val
XM_011511982.1:c.-433-19569A>C (C2orf88)	XP_011510284.1:n.-433-19569A>C
XM_011511986.1:c.-234-19569A>C (C2orf88)	XP_011510288.1:n.-234-19569A>C
XM_011511986.2:c.-234-19569A>C (C2orf88)	XP_011510288.1:n.-234-19569A>C
NM_005259.3:c.424T>G (MSTN) MANE Select	NP_005250.1:p.Phe142Val