Canonical Allele Identifier: CA13418915

Gene: MYRF TMEM258

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61770057T>G , CM000673.2:g.61770057T>G	GRCh38
NC_000011.9:g.61537529T>G , CM000673.1:g.61537529T>G	GRCh37
NC_000011.8:g.61294105T>G	NCBI36
NG_047038.1:g.22421T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001127392.3:c.461-189T>G (MYRF) MANE Select	NP_001120864.1:n.461-189T>G
ENST00000278836.10:c.461-189T>G (MYRF) MANE Select	ENSP00000278836.4:n.461-189T>G
NM_001127392.2:c.461-189T>G (MYRF)	NP_001120864.1:n.461-189T>G
NM_013279.3:c.434-189T>G (MYRF)	NP_037411.1:n.434-189T>G
NM_013279.4:c.434-189T>G (MYRF)	NP_037411.1:n.434-189T>G
ENST00000265460.9:c.434-189T>G (MYRF)	ENSP00000265460.5:n.434-189T>G
ENST00000278836.9:c.461-189T>G (MYRF)	ENSP00000278836.4:n.461-189T>G
ENST00000535042.1:n.649-1284A>C (TMEM258)
ENST00000675319.1:c.106-1443T>G (MYRF)
XM_005274222.1:c.461-189T>G (MYRF)	XP_005274279.1:n.461-189T>G
XM_005274223.1:c.461-189T>G (MYRF)	XP_005274280.1:n.461-189T>G
XM_005274224.1:c.461-189T>G (MYRF)	XP_005274281.1:n.461-189T>G
XM_005274225.1:c.461-189T>G (MYRF)	XP_005274282.1:n.461-189T>G
XM_005274226.1:c.461-189T>G (MYRF)	XP_005274283.1:n.461-189T>G
XM_005274227.1:c.461-189T>G (MYRF)	XP_005274284.1:n.461-189T>G
XM_005274228.1:c.454-335T>G (MYRF)	XP_005274285.1:n.454-335T>G
XM_011545234.1:c.4-335T>G (MYRF)	XP_011543536.1:n.4-335T>G
XM_011545234.2:c.4-335T>G (MYRF)	XP_011543536.1:n.4-335T>G
XM_024448677.1:c.20-189T>G (MYRF)	XP_024304445.1:n.20-189T>G