Canonical Allele Identifier: CA10743107
Gene: SELP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169621855A>G , CM000663.2:g.169621855A>G GRCh38
NC_000001.10:g.169591093A>G , CM000663.1:g.169591093A>G GRCh37
NC_000001.9:g.167857717A>G NCBI36
NG_012125.1:g.13285T>C
NG_012125.2:g.13285T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263686.11:c.4-2636T>C MANE Select ENSP00000263686.5:n.4-2636T>C
ENST00000263686.10:c.4-2636T>C ENSP00000263686.5:n.4-2636T>C
ENST00000367786.6:c.4-2636T>C ENSP00000356760.1:n.4-2636T>C
ENST00000367788.6:c.4-2636T>C ENSP00000356762.1:n.4-2636T>C
ENST00000367795.2:c.4-2636T>C ENSP00000356769.2:n.4-2636T>C
ENST00000458599.6:c.4-2636T>C ENSP00000399368.2:n.4-2636T>C
NM_003005.3:c.4-2636T>C NP_002996.2:n.4-2636T>C
XM_005245435.1:c.4-2636T>C XP_005245492.1:n.4-2636T>C
XM_005245436.2:c.4-2636T>C XP_005245493.1:n.4-2636T>C
XM_005245438.1:c.4-2636T>C XP_005245495.1:n.4-2636T>C
XM_005245439.1:c.4-2636T>C XP_005245496.1:n.4-2636T>C
XM_005245440.1:c.4-2636T>C XP_005245497.1:n.4-2636T>C
XM_005245435.2:c.4-2636T>C XP_005245492.1:n.4-2636T>C
XM_005245436.4:c.4-2636T>C XP_005245493.1:n.4-2636T>C
XM_005245438.2:c.4-2636T>C XP_005245495.1:n.4-2636T>C
XM_005245439.2:c.4-2636T>C XP_005245496.1:n.4-2636T>C
XM_005245440.2:c.4-2636T>C XP_005245497.1:n.4-2636T>C
NM_003005.4:c.4-2636T>C MANE Select NP_002996.2:n.4-2636T>C
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