Canonical Allele Identifier: CA2694681105

Gene: ELF4

Linked Data

• gnomAD v4: X-130065772-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130065772A>G , CM000685.2:g.130065772A>G	GRCh38
NC_000023.10:g.129199747A>G , CM000685.1:g.129199747A>G	GRCh37
NC_000023.9:g.129027428A>G	NCBI36
NG_016388.1:g.49942T>C , LRG_335:g.49942T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308167.10:c.*949T>C MANE Select	ENSP00000311280.6:n.*949T>C
ENST00000308167.9:c.*949T>C	ENSP00000311280.5:n.*949T>C
ENST00000335997.11:c.*949T>C	ENSP00000338608.7:n.*949T>C
ENST00000615377.4:c.*949T>C	ENSP00000478297.1:n.*949T>C
NM_001127197.1:c.*949T>C	NP_001120669.1:n.*949T>C
NM_001421.3:c.*949T>C , LRG_335t1:c.*949T>C	NP_001412.1:n.*949T>C
XM_005262389.2:c.*949T>C	XP_005262446.1:n.*949T>C
XM_011531307.1:c.*949T>C	XP_011529609.1:n.*949T>C
XM_011531308.1:c.*949T>C	XP_011529610.1:n.*949T>C
XM_005262389.3:c.*949T>C	XP_005262446.1:n.*949T>C
XM_011531307.3:c.*949T>C	XP_011529609.1:n.*949T>C
XM_011531308.3:c.*949T>C	XP_011529610.1:n.*949T>C
NM_001127197.2:c.*949T>C	NP_001120669.1:n.*949T>C
NM_001421.4:c.*949T>C MANE Select	NP_001412.1:n.*949T>C