Canonical Allele Identifier: CA2662349035

Gene: MSTN C2orf88

Linked Data

• gnomAD v4: 2-190060512-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190060518_190060519del , CM000664.2:g.190060518_190060519del	GRCh38
NC_000002.11:g.190925244_190925245del , CM000664.1:g.190925244_190925245del	GRCh37
NC_000002.10:g.190633489_190633490del	NCBI36
NG_009800.1:g.7216_7217del , LRG_200:g.7216_7217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.374-79_374-78del (MSTN) MANE Select	ENSP00000260950.3:n.374-79_374-78del
ENST00000260950.4:c.374-79_374-78del (MSTN)	ENSP00000260950.3:n.374-79_374-78del
ENST00000478197.1:n.220-18705_220-18704del (C2orf88)
ENST00000495546.1:n.202-19436_202-19435del (C2orf88)
NM_005259.2:c.374-79_374-78del , LRG_200t1:c.374-79_374-78del (MSTN)	NP_005250.1:n.374-79_374-78del
XM_005246905.1:c.-359-19436_-359-19435del (C2orf88)	XP_005246962.1:n.-359-19436_-359-19435del
XM_011510958.1:c.-11-79_-11-78del (MSTN)	XP_011509260.1:n.-11-79_-11-78del
XM_011511982.1:c.-433-19436_-433-19435del (C2orf88)	XP_011510284.1:n.-433-19436_-433-19435del
XM_011511986.1:c.-234-19436_-234-19435del (C2orf88)	XP_011510288.1:n.-234-19436_-234-19435del
XM_011511986.2:c.-234-19436_-234-19435del (C2orf88)	XP_011510288.1:n.-234-19436_-234-19435del
NM_005259.3:c.374-79_374-78del (MSTN) MANE Select	NP_005250.1:n.374-79_374-78del