Canonical Allele Identifier: CA362676072
Community Standard Title: NM_004415.4(DSP):c.170+1G>A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7542086G>A , CM000668.2:g.7542086G>A GRCh38
NC_000006.11:g.7542319G>A , CM000668.1:g.7542319G>A GRCh37
NC_000006.10:g.7487318G>A NCBI36
NG_008803.1:g.5450G>A , LRG_423:g.5450G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004415.4:c.170+1G>A (DSP) MANE Select NP_004406.2:n.170+1G>A
ENST00000379802.8:c.170+1G>A (DSP) MANE Select ENSP00000369129.3:n.170+1G>A
NM_001008844.1:c.170+1G>A (DSP) NP_001008844.1:n.170+1G>A
NM_001008844.2:c.170+1G>A (DSP) NP_001008844.1:n.170+1G>A
NM_001008844.3:c.170+1G>A (DSP) NP_001008844.1:n.170+1G>A
NM_001319034.1:c.170+1G>A (DSP) NP_001305963.1:n.170+1G>A
NM_001319034.2:c.170+1G>A (DSP) NP_001305963.1:n.170+1G>A
NM_004415.2:c.170+1G>A , LRG_423t1:c.170+1G>A (DSP) NP_004406.2:n.170+1G>A
NM_004415.3:c.170+1G>A (DSP) NP_004406.2:n.170+1G>A
ENST00000379802.7:c.170+1G>A (DSP) ENSP00000369129.3:n.170+1G>A
ENST00000418664.2:c.170+1G>A (DSP) ENSP00000396591.2:n.170+1G>A
ENST00000683563.1:n.62+1G>A (DSP)
ENST00000683682.1:c.65+1G>A (DSP) ENSP00000508162.1:n.65+1G>A
ENST00000683682.2:c.170+1G>A (DSP) ENSP00000508162.2:n.170+1G>A
ENST00000710359.1:c.170+1G>A (DSP) ENSP00000518230.1:n.170+1G>A
XM_011514323.1:c.170+1G>A (DSP) XP_011512625.1:n.170+1G>A
XR_241971.2:n.268+685C>T (DSP-AS1)
XR_241971.3:n.269+685C>T (DSP-AS1)