Canonical Allele Identifier: CA1206165628
Gene: SELP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169611210A= , CM000663.2:g.169611210A= GRCh38
NC_000001.10:g.169580448A= , CM000663.1:g.169580448A= GRCh37
NC_000001.9:g.167847072A= NCBI36
NG_012125.1:g.23930T=
NG_012125.2:g.23930T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263686.11:c.1147+282T= MANE Select ENSP00000263686.5:n.1147+282T=
ENST00000263686.10:c.1147+282T= ENSP00000263686.5:n.1147+282T=
ENST00000367786.6:c.961+1007T= ENSP00000356760.1:n.961+1007T=
ENST00000367788.6:c.961+282T= ENSP00000356762.1:n.961+282T=
ENST00000367795.2:c.961+1007T= ENSP00000356769.2:n.961+1007T=
ENST00000426706.6:c.1144+282T= ENSP00000391694.2:n.1144+282T=
ENST00000458599.6:c.961+1007T= ENSP00000399368.2:n.961+1007T=
NM_003005.3:c.1147+282T= NP_002996.2:n.1147+282T=
XM_005245435.1:c.1147+282T= XP_005245492.1:n.1147+282T=
XM_005245436.2:c.1147+282T= XP_005245493.1:n.1147+282T=
XM_005245438.1:c.1147+282T= XP_005245495.1:n.1147+282T=
XM_005245439.1:c.1147+282T= XP_005245496.1:n.1147+282T=
XM_005245440.1:c.961+1007T= XP_005245497.1:n.961+1007T=
XM_005245435.2:c.1147+282T= XP_005245492.1:n.1147+282T=
XM_005245436.4:c.1147+282T= XP_005245493.1:n.1147+282T=
XM_005245438.2:c.1147+282T= XP_005245495.1:n.1147+282T=
XM_005245439.2:c.1147+282T= XP_005245496.1:n.1147+282T=
XM_005245440.2:c.961+1007T= XP_005245497.1:n.961+1007T=
NM_003005.4:c.1147+282T= MANE Select NP_002996.2:n.1147+282T=