Canonical Allele Identifier: CA1315870344

Gene: MSTN C2orf88

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260950.5:c.748-1048T>G (MSTN) MANE Select	ENSP00000260950.3:n.748-1048T>G
ENST00000260950.4:c.748-1048T>G (MSTN)	ENSP00000260950.3:n.748-1048T>G
ENST00000478197.1:n.220-20537A>C (C2orf88)
ENST00000495546.1:n.202-21268A>C (C2orf88)
NM_005259.2:c.748-1048T>G , LRG_200t1:c.748-1048T>G (MSTN)	NP_005250.1:n.748-1048T>G
XM_005246905.1:c.-359-21268A>C (C2orf88)	XP_005246962.1:n.-359-21268A>C
XM_011510958.1:c.364-1048T>G (MSTN)	XP_011509260.1:n.364-1048T>G
XM_011511982.1:c.-433-21268A>C (C2orf88)	XP_011510284.1:n.-433-21268A>C
XM_011511986.1:c.-234-21268A>C (C2orf88)	XP_011510288.1:n.-234-21268A>C
XM_011511986.2:c.-234-21268A>C (C2orf88)	XP_011510288.1:n.-234-21268A>C
NM_005259.3:c.748-1048T>G (MSTN) MANE Select	NP_005250.1:n.748-1048T>G