Canonical Allele Identifier: CA2255058003
Gene: NSRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30117071G= , CM000679.2:g.30117071G= GRCh38
NC_000017.10:g.28444089G= , CM000679.1:g.28444089G= GRCh37
NC_000017.9:g.25468215G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000247026.10:c.20+208G= MANE Select ENSP00000247026.5:n.20+208G=
ENST00000247026.9:c.20+208G= ENSP00000247026.5:n.20+208G=
ENST00000394826.8:c.20+208G= ENSP00000378303.4:n.20+208G=
ENST00000475652.5:c.20+208G= ENSP00000464569.1:n.20+208G=
ENST00000479218.6:c.20+208G= ENSP00000466640.1:n.20+208G=
ENST00000540900.7:n.321+208G=
ENST00000577289.6:n.45+208G=
ENST00000583301.5:n.25+208G=
ENST00000584154.5:c.20+208G= ENSP00000462820.1:n.20+208G=
ENST00000584317.5:c.20+208G= ENSP00000463722.1:n.20+208G=
ENST00000584423.5:c.20+208G= ENSP00000464237.1:n.20+208G=
ENST00000585881.5:c.-310G= ENSP00000465442.1:n.-310G=
ENST00000612959.4:c.-49+208G= ENSP00000477862.1:n.-49+208G=
NM_001261467.1:c.-49+208G= NP_001248396.1:n.-49+208G=
NM_032141.3:c.20+208G= NP_115517.1:n.20+208G=
XM_011525345.1:c.20+208G= XP_011523647.1:n.20+208G=
XR_934651.1:n.682+321C=
XM_011525345.2:c.20+208G= XP_011523647.1:n.20+208G=
NM_032141.4:c.20+208G= MANE Select NP_115517.1:n.20+208G=
NM_001261467.2:c.-49+208G= NP_001248396.1:n.-49+208G=