Canonical Allele Identifier: CA362674774
Gene: DSP HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.7566622C>A (hg19) chr6:g.7566389C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7566389C>A , CM000668.2:g.7566389C>A GRCh38
NC_000006.11:g.7566622C>A , CM000668.1:g.7566622C>A GRCh37
NC_000006.10:g.7511621C>A NCBI36
NG_008803.1:g.29753C>A , LRG_423:g.29753C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.952C>A ENSP00000518230.1:p.Gln318Lys
ENST00000682228.1:n.276C>A
ENST00000379802.8:c.952C>A MANE Select ENSP00000369129.3:p.Gln318Lys
ENST00000379802.7:c.952C>A ENSP00000369129.3:p.Gln318Lys
ENST00000418664.2:c.952C>A ENSP00000396591.2:p.Gln318Lys
NM_001008844.1:c.952C>A NP_001008844.1:p.Gln318Lys
NM_004415.2:c.952C>A , LRG_423t1:c.952C>A NP_004406.2:p.Gln318Lys
XM_011514323.1:c.952C>A XP_011512625.1:p.Gln318Lys
NM_001008844.2:c.952C>A NP_001008844.1:p.Gln318Lys
NM_001319034.1:c.952C>A NP_001305963.1:p.Gln318Lys
NM_004415.3:c.952C>A NP_004406.2:p.Gln318Lys
NM_004415.4:c.952C>A MANE Select NP_004406.2:p.Gln318Lys
NM_001008844.3:c.952C>A NP_001008844.1:p.Gln318Lys
NM_001319034.2:c.952C>A NP_001305963.1:p.Gln318Lys
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