Canonical Allele Identifier: CA2458270136

Gene: ELF4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130065841C= , CM000685.2:g.130065841C=	GRCh38
NC_000023.10:g.129199816C= , CM000685.1:g.129199816C=	GRCh37
NC_000023.9:g.129027497C=	NCBI36
NG_016388.1:g.49873G= , LRG_335:g.49873G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308167.10:c.*880G= MANE Select	ENSP00000311280.6:n.*880G=
ENST00000308167.9:c.*880G=	ENSP00000311280.5:n.*880G=
ENST00000335997.11:c.*880G=	ENSP00000338608.7:n.*880G=
ENST00000615377.4:c.*880G=	ENSP00000478297.1:n.*880G=
NM_001127197.1:c.*880G=	NP_001120669.1:n.*880G=
NM_001421.3:c.*880G= , LRG_335t1:c.*880G=	NP_001412.1:n.*880G=
XM_005262389.2:c.*880G=	XP_005262446.1:n.*880G=
XM_011531307.1:c.*880G=	XP_011529609.1:n.*880G=
XM_011531308.1:c.*880G=	XP_011529610.1:n.*880G=
XM_005262389.3:c.*880G=	XP_005262446.1:n.*880G=
XM_011531307.3:c.*880G=	XP_011529609.1:n.*880G=
XM_011531308.3:c.*880G=	XP_011529610.1:n.*880G=
NM_001127197.2:c.*880G=	NP_001120669.1:n.*880G=
NM_001421.4:c.*880G= MANE Select	NP_001412.1:n.*880G=