Canonical Allele Identifier: CA248392703
Gene: ELF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40983974A>G , CM000675.2:g.40983974A>G GRCh38
NC_000013.10:g.41558110A>G , CM000675.1:g.41558110A>G GRCh37
NC_000013.9:g.40456110A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239882.7:c.-228-1692T>C MANE Select ENSP00000239882.3:n.-228-1692T>C
ENST00000239882.6:c.-228-1692T>C ENSP00000239882.3:n.-228-1692T>C
ENST00000405737.2:c.-228-1692T>C ENSP00000384135.2:n.-228-1692T>C
ENST00000442101.5:c.-323-1692T>C ENSP00000405580.2:n.-323-1692T>C
NM_172373.3:c.-228-1692T>C NP_758961.1:n.-228-1692T>C
XM_005266277.2:c.-228-1692T>C XP_005266334.1:n.-228-1692T>C
XM_011534950.1:c.-228-1692T>C XP_011533252.1:n.-228-1692T>C
XM_011534951.1:c.-524-1692T>C XP_011533253.1:n.-524-1692T>C
XM_011534952.1:c.-228-1692T>C XP_011533254.1:n.-228-1692T>C
XM_005266277.4:c.-228-1692T>C XP_005266334.1:n.-228-1692T>C
XM_011534951.3:c.-524-1692T>C XP_011533253.1:n.-524-1692T>C
NM_172373.4:c.-228-1692T>C MANE Select NP_758961.1:n.-228-1692T>C
NM_001370329.1:c.-524-1692T>C NP_001357258.1:n.-524-1692T>C
NM_001370330.1:c.-228-1692T>C NP_001357259.1:n.-228-1692T>C
NM_001370332.1:c.-228-1692T>C NP_001357261.1:n.-228-1692T>C
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