Canonical Allele Identifier: CA1451375696
Gene: RELL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.37649533A= , CM000666.2:g.37649533A= GRCh38
NC_000004.11:g.37651155A= , CM000666.1:g.37651155A= GRCh37
NC_000004.10:g.37327550A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454158.7:c.89-33T= MANE Select ENSP00000398778.2:n.89-33T=
ENST00000314117.8:c.89-33T= ENSP00000313385.4:n.89-33T=
ENST00000454158.6:c.89-33T= ENSP00000398778.2:n.89-33T=
ENST00000512114.1:c.152-33T= ENSP00000424031.1:n.152-33T=
NM_001085399.1:c.89-33T= NP_001078868.1:n.89-33T=
NM_001085400.1:c.89-33T= NP_001078869.1:n.89-33T=
XR_427509.1:n.179-33T=
XR_925167.1:n.179-33T=
XR_925168.1:n.179-33T=
XR_925169.1:n.179-33T=
XR_925170.1:n.179-33T=
XM_017008590.2:c.-453-33T= XP_016864079.1:n.-453-33T=
XR_002959758.1:n.205-33T=
NM_001085400.2:c.89-33T= MANE Select NP_001078869.1:n.89-33T=
NM_001085399.2:c.89-33T= NP_001078868.1:n.89-33T=