Canonical Allele Identifier: CA448716975
Gene: DSP HGNC NCBI

Linked Data

gnomAD v4: 6-7585200-G-C
MyVariant Identifiers: chr6:g.7585433G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585200G>C , CM000668.2:g.7585200G>C GRCh38
NC_000006.11:g.7585433G>C , CM000668.1:g.7585433G>C GRCh37
NC_000006.10:g.7530432G>C NCBI36
NG_008803.1:g.48564G>C , LRG_423:g.48564G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6609G>C ENSP00000518230.1:p.Thr2203=
ENST00000379802.8:c.7938G>C MANE Select ENSP00000369129.3:p.Thr2646=
ENST00000379802.7:c.7938G>C ENSP00000369129.3:p.Thr2646=
ENST00000418664.2:c.6141G>C ENSP00000396591.2:p.Thr2047=
NM_001008844.1:c.6141G>C NP_001008844.1:p.Thr2047=
NM_004415.2:c.7938G>C , LRG_423t1:c.7938G>C NP_004406.2:p.Thr2646=
XM_011514323.1:c.6609G>C XP_011512625.1:p.Thr2203=
NM_001008844.2:c.6141G>C NP_001008844.1:p.Thr2047=
NM_001319034.1:c.6609G>C NP_001305963.1:p.Thr2203=
NM_004415.3:c.7938G>C NP_004406.2:p.Thr2646=
NM_004415.4:c.7938G>C MANE Select NP_004406.2:p.Thr2646=
NM_001008844.3:c.6141G>C NP_001008844.1:p.Thr2047=
NM_001319034.2:c.6609G>C NP_001305963.1:p.Thr2203=