Canonical Allele Identifier: CA2838201186
Gene: ELAPOR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109158258T>G , CM000663.2:g.109158258T>G GRCh38
NC_000001.10:g.109700880T>G , CM000663.1:g.109700880T>G GRCh37
NC_000001.9:g.109502403T>G NCBI36
NG_032763.1:g.49296T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369939.8:c.154-3636T>G MANE Select ENSP00000358955.3:n.154-3636T>G
ENST00000369939.7:c.154-3636T>G ENSP00000358955.3:n.154-3636T>G
ENST00000457623.6:c.154-3636T>G ENSP00000393964.2:n.154-3636T>G
ENST00000490758.6:n.165-6241T>G
ENST00000526264.5:c.154-3636T>G ENSP00000435066.1:n.154-3636T>G
ENST00000527996.5:c.154-6241T>G ENSP00000432023.1:n.154-6241T>G
ENST00000529753.5:c.154-3636T>G ENSP00000434595.1:n.154-3636T>G
ENST00000531664.5:c.154-3636T>G ENSP00000431349.1:n.154-3636T>G
ENST00000533147.5:c.154-3636T>G ENSP00000431134.1:n.154-3636T>G
ENST00000534476.5:c.154-3636T>G ENSP00000432164.1:n.154-3636T>G
NM_001267048.1:c.154-3636T>G NP_001253977.1:n.154-3636T>G
NM_001284352.1:c.-32-6241T>G NP_001271281.1:n.-32-6241T>G
NM_020775.4:c.154-3636T>G NP_065826.2:n.154-3636T>G
XM_011541825.1:c.154-3636T>G XP_011540127.1:n.154-3636T>G
XM_011541826.1:c.154-3636T>G XP_011540128.1:n.154-3636T>G
XM_011541827.1:c.154-3636T>G XP_011540129.1:n.154-3636T>G
XM_011541825.2:c.154-3636T>G XP_011540127.1:n.154-3636T>G
XM_011541826.3:c.154-3636T>G XP_011540128.1:n.154-3636T>G
XM_011541827.2:c.154-3636T>G XP_011540129.1:n.154-3636T>G
XM_017001883.2:c.-694-3636T>G XP_016857372.1:n.-694-3636T>G
NM_020775.5:c.154-3636T>G MANE Select NP_065826.3:n.154-3636T>G
NM_001267048.2:c.154-3636T>G NP_001253977.2:n.154-3636T>G
NM_001284352.2:c.-32-6241T>G NP_001271281.1:n.-32-6241T>G