Canonical Allele Identifier: CA4160448

Gene: MIOS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7572930C>A , CM000669.2:g.7572930C>A	GRCh38
NC_000007.13:g.7612561C>A , CM000669.1:g.7612561C>A	GRCh37
NC_000007.12:g.7579086C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_019005.4:c.455C>A MANE Select	NP_061878.3:p.Thr152Asn
ENST00000340080.9:c.455C>A MANE Select	ENSP00000339881.4:p.Thr152Asn
NM_001370076.1:c.455C>A	NP_001357005.1:p.Thr152Asn
NM_001370077.1:c.455C>A	NP_001357006.1:p.Thr152Asn
NM_001370078.1:c.455C>A	NP_001357007.1:p.Thr152Asn
NM_001370080.1:c.455C>A	NP_001357009.1:p.Thr152Asn
NM_019005.3:c.455C>A	NP_061878.3:p.Thr152Asn
NR_163250.1:n.684C>A
ENST00000340080.8:c.455C>A	ENSP00000339881.4:p.Thr152Asn
ENST00000405785.5:c.455C>A	ENSP00000384088.1:p.Thr152Asn
ENST00000456533.1:c.455C>A	ENSP00000410752.1:p.Thr152Asn
XM_005249780.2:c.455C>A	XP_005249837.1:p.Thr152Asn
XM_005249780.3:c.455C>A	XP_005249837.1:p.Thr152Asn
XM_005249781.2:c.455C>A	XP_005249838.1:p.Thr152Asn
XM_005249781.3:c.455C>A	XP_005249838.1:p.Thr152Asn
XM_005249782.2:c.455C>A	XP_005249839.1:p.Thr152Asn
XM_005249782.3:c.455C>A	XP_005249839.1:p.Thr152Asn
XM_005249783.2:c.455C>A	XP_005249840.1:p.Thr152Asn
XM_005249784.2:c.455C>A	XP_005249841.1:p.Thr152Asn
XM_005249784.4:c.455C>A	XP_005249841.1:p.Thr152Asn
XM_011515432.1:c.455C>A	XP_011513734.1:p.Thr152Asn
XM_011515432.2:c.455C>A	XP_011513734.1:p.Thr152Asn
XM_017012362.2:c.-1122C>A	XP_016867851.1:n.-1122C>A
XM_024446803.1:c.455C>A	XP_024302571.1:p.Thr152Asn