Canonical Allele Identifier: CA13418921

Gene: MYRF TMEM258

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61785208G>T , CM000673.2:g.61785208G>T	GRCh38
NC_000011.9:g.61552680G>T , CM000673.1:g.61552680G>T	GRCh37
NC_000011.8:g.61309256G>T	NCBI36
NG_047038.1:g.37572G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278836.10:c.3301-592G>T (MYRF) MANE Select	ENSP00000278836.4:n.3301-592G>T
ENST00000675319.1:c.2666-592G>T (MYRF)
ENST00000675345.1:c.1153-592G>T (MYRF)	ENSP00000502028.1:n.1153-592G>T
ENST00000675792.1:c.287-505G>T (MYRF)
ENST00000265460.9:c.3181-592G>T (MYRF)	ENSP00000265460.5:n.3181-592G>T
ENST00000278836.9:c.3301-592G>T (MYRF)	ENSP00000278836.4:n.3301-592G>T
ENST00000389602.4:c.1459-592G>T (MYRF)	ENSP00000374253.4:n.1459-592G>T
ENST00000535042.1:n.248+4577C>A (TMEM258)
ENST00000539361.1:n.3022G>T (MYRF)
NM_001127392.2:c.3301-592G>T (MYRF)	NP_001120864.1:n.3301-592G>T
NM_013279.3:c.3181-592G>T (MYRF)	NP_037411.1:n.3181-592G>T
XM_005274222.1:c.3304-592G>T (MYRF)	XP_005274279.1:n.3304-592G>T
XM_005274223.1:c.3289-592G>T (MYRF)	XP_005274280.1:n.3289-592G>T
XM_005274224.1:c.3286-592G>T (MYRF)	XP_005274281.1:n.3286-592G>T
XM_005274225.1:c.3223-592G>T (MYRF)	XP_005274282.1:n.3223-592G>T
XM_005274226.1:c.3220-592G>T (MYRF)	XP_005274283.1:n.3220-592G>T
XM_005274227.1:c.3208-592G>T (MYRF)	XP_005274284.1:n.3208-592G>T
XM_005274228.1:c.3151-592G>T (MYRF)	XP_005274285.1:n.3151-592G>T
XM_011545234.1:c.2701-592G>T (MYRF)	XP_011543536.1:n.2701-592G>T
XM_011545234.2:c.2701-592G>T (MYRF)	XP_011543536.1:n.2701-592G>T
XM_024448677.1:c.2863-592G>T (MYRF)	XP_024304445.1:n.2863-592G>T
NM_001127392.3:c.3301-592G>T (MYRF) MANE Select	NP_001120864.1:n.3301-592G>T
NM_013279.4:c.3181-592G>T (MYRF)	NP_037411.1:n.3181-592G>T