Canonical Allele Identifier: CA2592473666
Gene: NSRP1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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