Canonical Allele Identifier: CA335108868

Gene: ELF4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130069575A>G , CM000685.2:g.130069575A>G	GRCh38
NC_000023.10:g.129203550A>G , CM000685.1:g.129203550A>G	GRCh37
NC_000023.9:g.129031231A>G	NCBI36
NG_016388.1:g.46139T>C , LRG_335:g.46139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308167.10:c.912T>C MANE Select	ENSP00000311280.6:p.Asp304=
ENST00000308167.9:c.912T>C	ENSP00000311280.5:p.Asp304=
ENST00000335997.11:c.912T>C	ENSP00000338608.7:p.Asp304=
ENST00000615377.4:c.912T>C	ENSP00000478297.1:p.Asp304=
NM_001127197.1:c.912T>C	NP_001120669.1:p.Asp304=
NM_001421.3:c.912T>C , LRG_335t1:c.912T>C	NP_001412.1:p.Asp304=
XM_005262389.2:c.912T>C	XP_005262446.1:p.Asp304=
XM_011531307.1:c.708T>C	XP_011529609.1:p.Asp236=
XM_011531308.1:c.681T>C	XP_011529610.1:p.Asp227=
XM_005262389.3:c.912T>C	XP_005262446.1:p.Asp304=
XM_011531307.3:c.708T>C	XP_011529609.1:p.Asp236=
XM_011531308.3:c.681T>C	XP_011529610.1:p.Asp227=
NM_001127197.2:c.912T>C	NP_001120669.1:p.Asp304=
NM_001421.4:c.912T>C MANE Select	NP_001412.1:p.Asp304=