Canonical Allele Identifier: CA2636995255

Gene: NSRP1

Linked Data

• gnomAD v4: 17-30117066-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30117066A>G , CM000679.2:g.30117066A>G	GRCh38
NC_000017.10:g.28444084A>G , CM000679.1:g.28444084A>G	GRCh37
NC_000017.9:g.25468210A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000247026.10:c.20+203A>G MANE Select	ENSP00000247026.5:n.20+203A>G
ENST00000247026.9:c.20+203A>G	ENSP00000247026.5:n.20+203A>G
ENST00000394826.8:c.20+203A>G	ENSP00000378303.4:n.20+203A>G
ENST00000475652.5:c.20+203A>G	ENSP00000464569.1:n.20+203A>G
ENST00000479218.6:c.20+203A>G	ENSP00000466640.1:n.20+203A>G
ENST00000540900.7:n.321+203A>G
ENST00000577289.6:n.45+203A>G
ENST00000583301.5:n.25+203A>G
ENST00000584154.5:c.20+203A>G	ENSP00000462820.1:n.20+203A>G
ENST00000584317.5:c.20+203A>G	ENSP00000463722.1:n.20+203A>G
ENST00000584423.5:c.20+203A>G	ENSP00000464237.1:n.20+203A>G
ENST00000585881.5:c.-315A>G	ENSP00000465442.1:n.-315A>G
ENST00000612959.4:c.-49+203A>G	ENSP00000477862.1:n.-49+203A>G
NM_001261467.1:c.-49+203A>G	NP_001248396.1:n.-49+203A>G
NM_032141.3:c.20+203A>G	NP_115517.1:n.20+203A>G
XM_011525345.1:c.20+203A>G	XP_011523647.1:n.20+203A>G
XR_934651.1:n.682+326T>C
XM_011525345.2:c.20+203A>G	XP_011523647.1:n.20+203A>G
NM_032141.4:c.20+203A>G MANE Select	NP_115517.1:n.20+203A>G
NM_001261467.2:c.-49+203A>G	NP_001248396.1:n.-49+203A>G