Canonical Allele Identifier: CA362675731
Community Standard Title: NM_004415.4(DSP):c.84C>A (p.Tyr28Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541999C>A , CM000668.2:g.7541999C>A GRCh38
NC_000006.11:g.7542232C>A , CM000668.1:g.7542232C>A GRCh37
NC_000006.10:g.7487231C>A NCBI36
NG_008803.1:g.5363C>A , LRG_423:g.5363C>A

Transcript Alleles

HGVS Amino-acid Change
NM_004415.4:c.84C>A (DSP) MANE Select NP_004406.2:p.Tyr28Ter
ENST00000379802.8:c.84C>A (DSP) MANE Select ENSP00000369129.3:p.Tyr28Ter
NM_001008844.1:c.84C>A (DSP) NP_001008844.1:p.Tyr28Ter
NM_001008844.2:c.84C>A (DSP) NP_001008844.1:p.Tyr28Ter
NM_001008844.3:c.84C>A (DSP) NP_001008844.1:p.Tyr28Ter
NM_001319034.1:c.84C>A (DSP) NP_001305963.1:p.Tyr28Ter
NM_001319034.2:c.84C>A (DSP) NP_001305963.1:p.Tyr28Ter
NM_004415.2:c.84C>A , LRG_423t1:c.84C>A (DSP) NP_004406.2:p.Tyr28Ter
NM_004415.3:c.84C>A (DSP) NP_004406.2:p.Tyr28Ter
ENST00000379802.7:c.84C>A (DSP) ENSP00000369129.3:p.Tyr28Ter
ENST00000418664.2:c.84C>A (DSP) ENSP00000396591.2:p.Tyr28Ter
ENST00000683682.2:c.84C>A (DSP) ENSP00000508162.2:p.Tyr28Ter
ENST00000710359.1:c.84C>A (DSP) ENSP00000518230.1:p.Tyr28Ter
XM_011514323.1:c.84C>A (DSP) XP_011512625.1:p.Tyr28Ter
XR_241971.2:n.268+772G>T (DSP-AS1)
XR_241971.3:n.269+772G>T (DSP-AS1)