Canonical Allele Identifier: CA1608614587
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7579713_7579714delinsAG , CM000668.2:g.7579713_7579714delinsAG GRCh38
NC_000006.11:g.7579946_7579947delinsAG , CM000668.1:g.7579946_7579947delinsAG GRCh37
NC_000006.10:g.7524945_7524946delinsAG NCBI36
NG_008803.1:g.43077_43078delinsAG , LRG_423:g.43077_43078delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.3523_3524delinsAG ENSP00000518230.1:p.Arg1175=
ENST00000379802.8:c.3523_3524delinsAG MANE Select ENSP00000369129.3:p.Arg1175=
ENST00000379802.7:c.3523_3524delinsAG ENSP00000369129.3:p.Arg1175=
ENST00000418664.2:c.3523_3524delinsAG ENSP00000396591.2:p.Arg1175=
NM_001008844.1:c.3523_3524delinsAG NP_001008844.1:p.Arg1175=
NM_004415.2:c.3523_3524delinsAG , LRG_423t1:c.3523_3524delinsAG NP_004406.2:p.Arg1175=
XM_011514323.1:c.3523_3524delinsAG XP_011512625.1:p.Arg1175=
NM_001008844.2:c.3523_3524delinsAG NP_001008844.1:p.Arg1175=
NM_001319034.1:c.3523_3524delinsAG NP_001305963.1:p.Arg1175=
NM_004415.3:c.3523_3524delinsAG NP_004406.2:p.Arg1175=
NM_004415.4:c.3523_3524delinsAG MANE Select NP_004406.2:p.Arg1175=
NM_001008844.3:c.3523_3524delinsAG NP_001008844.1:p.Arg1175=
NM_001319034.2:c.3523_3524delinsAG NP_001305963.1:p.Arg1175=