Canonical Allele Identifier: CA362675874
Community Standard Title: NM_004415.4(DSP):c.122A>G (p.Tyr41Cys)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7542037A>G , CM000668.2:g.7542037A>G GRCh38
NC_000006.11:g.7542270A>G , CM000668.1:g.7542270A>G GRCh37
NC_000006.10:g.7487269A>G NCBI36
NG_008803.1:g.5401A>G , LRG_423:g.5401A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004415.4:c.122A>G (DSP) MANE Select NP_004406.2:p.Tyr41Cys
ENST00000379802.8:c.122A>G (DSP) MANE Select ENSP00000369129.3:p.Tyr41Cys
NM_001008844.1:c.122A>G (DSP) NP_001008844.1:p.Tyr41Cys
NM_001008844.2:c.122A>G (DSP) NP_001008844.1:p.Tyr41Cys
NM_001008844.3:c.122A>G (DSP) NP_001008844.1:p.Tyr41Cys
NM_001319034.1:c.122A>G (DSP) NP_001305963.1:p.Tyr41Cys
NM_001319034.2:c.122A>G (DSP) NP_001305963.1:p.Tyr41Cys
NM_004415.2:c.122A>G , LRG_423t1:c.122A>G (DSP) NP_004406.2:p.Tyr41Cys
NM_004415.3:c.122A>G (DSP) NP_004406.2:p.Tyr41Cys
ENST00000379802.7:c.122A>G (DSP) ENSP00000369129.3:p.Tyr41Cys
ENST00000418664.2:c.122A>G (DSP) ENSP00000396591.2:p.Tyr41Cys
ENST00000683563.1:n.14A>G (DSP)
ENST00000683682.1:c.17A>G (DSP) ENSP00000508162.1:p.Tyr6Cys
ENST00000683682.2:c.122A>G (DSP) ENSP00000508162.2:p.Tyr41Cys
ENST00000710359.1:c.122A>G (DSP) ENSP00000518230.1:p.Tyr41Cys
XM_011514323.1:c.122A>G (DSP) XP_011512625.1:p.Tyr41Cys
XR_241971.2:n.268+734T>C (DSP-AS1)
XR_241971.3:n.269+734T>C (DSP-AS1)