Canonical Allele Identifier: CA2458270140

Gene: ELF4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130065863A= , CM000685.2:g.130065863A=	GRCh38
NC_000023.10:g.129199838A= , CM000685.1:g.129199838A=	GRCh37
NC_000023.9:g.129027519A=	NCBI36
NG_016388.1:g.49851T= , LRG_335:g.49851T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308167.10:c.*858T= MANE Select	ENSP00000311280.6:n.*858T=
ENST00000308167.9:c.*858T=	ENSP00000311280.5:n.*858T=
ENST00000335997.11:c.*858T=	ENSP00000338608.7:n.*858T=
ENST00000615377.4:c.*858T=	ENSP00000478297.1:n.*858T=
NM_001127197.1:c.*858T=	NP_001120669.1:n.*858T=
NM_001421.3:c.*858T= , LRG_335t1:c.*858T=	NP_001412.1:n.*858T=
XM_005262389.2:c.*858T=	XP_005262446.1:n.*858T=
XM_011531307.1:c.*858T=	XP_011529609.1:n.*858T=
XM_011531308.1:c.*858T=	XP_011529610.1:n.*858T=
XM_005262389.3:c.*858T=	XP_005262446.1:n.*858T=
XM_011531307.3:c.*858T=	XP_011529609.1:n.*858T=
XM_011531308.3:c.*858T=	XP_011529610.1:n.*858T=
NM_001127197.2:c.*858T=	NP_001120669.1:n.*858T=
NM_001421.4:c.*858T= MANE Select	NP_001412.1:n.*858T=