Canonical Allele Identifier: CA1206165612
Gene: SELP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169611190C= , CM000663.2:g.169611190C= GRCh38
NC_000001.10:g.169580428C= , CM000663.1:g.169580428C= GRCh37
NC_000001.9:g.167847052C= NCBI36
NG_012125.1:g.23950G=
NG_012125.2:g.23950G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263686.11:c.1147+302G= MANE Select ENSP00000263686.5:n.1147+302G=
ENST00000263686.10:c.1147+302G= ENSP00000263686.5:n.1147+302G=
ENST00000367786.6:c.961+1027G= ENSP00000356760.1:n.961+1027G=
ENST00000367788.6:c.961+302G= ENSP00000356762.1:n.961+302G=
ENST00000367795.2:c.961+1027G= ENSP00000356769.2:n.961+1027G=
ENST00000426706.6:c.1144+302G= ENSP00000391694.2:n.1144+302G=
ENST00000458599.6:c.961+1027G= ENSP00000399368.2:n.961+1027G=
NM_003005.3:c.1147+302G= NP_002996.2:n.1147+302G=
XM_005245435.1:c.1147+302G= XP_005245492.1:n.1147+302G=
XM_005245436.2:c.1147+302G= XP_005245493.1:n.1147+302G=
XM_005245438.1:c.1147+302G= XP_005245495.1:n.1147+302G=
XM_005245439.1:c.1147+302G= XP_005245496.1:n.1147+302G=
XM_005245440.1:c.961+1027G= XP_005245497.1:n.961+1027G=
XM_005245435.2:c.1147+302G= XP_005245492.1:n.1147+302G=
XM_005245436.4:c.1147+302G= XP_005245493.1:n.1147+302G=
XM_005245438.2:c.1147+302G= XP_005245495.1:n.1147+302G=
XM_005245439.2:c.1147+302G= XP_005245496.1:n.1147+302G=
XM_005245440.2:c.961+1027G= XP_005245497.1:n.961+1027G=
NM_003005.4:c.1147+302G= MANE Select NP_002996.2:n.1147+302G=