Canonical Allele Identifier: CA10514992

Gene: ELF4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130069380C>T , CM000685.2:g.130069380C>T	GRCh38
NC_000023.10:g.129203355C>T , CM000685.1:g.129203355C>T	GRCh37
NC_000023.9:g.129031036C>T	NCBI36
NG_016388.1:g.46334G>A , LRG_335:g.46334G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308167.10:c.1107G>A MANE Select	ENSP00000311280.6:p.Ser369=
ENST00000308167.9:c.1107G>A	ENSP00000311280.5:p.Ser369=
ENST00000335997.11:c.1107G>A	ENSP00000338608.7:p.Ser369=
ENST00000615377.4:c.1105G>A	ENSP00000478297.1:p.Ala369Thr
NM_001127197.1:c.1107G>A	NP_001120669.1:p.Ser369=
NM_001421.3:c.1107G>A , LRG_335t1:c.1107G>A	NP_001412.1:p.Ser369=
XM_005262389.2:c.1107G>A	XP_005262446.1:p.Ser369=
XM_011531307.1:c.903G>A	XP_011529609.1:p.Ser301=
XM_011531308.1:c.876G>A	XP_011529610.1:p.Ser292=
XM_005262389.3:c.1107G>A	XP_005262446.1:p.Ser369=
XM_011531307.3:c.903G>A	XP_011529609.1:p.Ser301=
XM_011531308.3:c.876G>A	XP_011529610.1:p.Ser292=
NM_001127197.2:c.1107G>A	NP_001120669.1:p.Ser369=
NM_001421.4:c.1107G>A MANE Select	NP_001412.1:p.Ser369=