Canonical Allele Identifier: CA2694681099
Gene: ELF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.130065758C>A , CM000685.2:g.130065758C>A GRCh38
NC_000023.10:g.129199733C>A , CM000685.1:g.129199733C>A GRCh37
NC_000023.9:g.129027414C>A NCBI36
NG_016388.1:g.49956G>T , LRG_335:g.49956G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308167.10:c.*963G>T MANE Select ENSP00000311280.6:n.*963G>T
ENST00000308167.9:c.*963G>T ENSP00000311280.5:n.*963G>T
ENST00000335997.11:c.*963G>T ENSP00000338608.7:n.*963G>T
ENST00000615377.4:c.*963G>T ENSP00000478297.1:n.*963G>T
NM_001127197.1:c.*963G>T NP_001120669.1:n.*963G>T
NM_001421.3:c.*963G>T , LRG_335t1:c.*963G>T NP_001412.1:n.*963G>T
XM_005262389.2:c.*963G>T XP_005262446.1:n.*963G>T
XM_011531307.1:c.*963G>T XP_011529609.1:n.*963G>T
XM_011531308.1:c.*963G>T XP_011529610.1:n.*963G>T
XM_005262389.3:c.*963G>T XP_005262446.1:n.*963G>T
XM_011531307.3:c.*963G>T XP_011529609.1:n.*963G>T
XM_011531308.3:c.*963G>T XP_011529610.1:n.*963G>T
NM_001127197.2:c.*963G>T NP_001120669.1:n.*963G>T
NM_001421.4:c.*963G>T MANE Select NP_001412.1:n.*963G>T