Canonical Allele Identifier: CA1608616199
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585843_7585844delinsTC , CM000668.2:g.7585843_7585844delinsTC GRCh38
NC_000006.11:g.7586076_7586077delinsTC , CM000668.1:g.7586076_7586077delinsTC GRCh37
NC_000006.10:g.7531075_7531076delinsTC NCBI36
NG_008803.1:g.49207_49208delinsTC , LRG_423:g.49207_49208delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.7252_7253delinsTC ENSP00000518230.1:p.Ser2418=
ENST00000379802.8:c.8581_8582delinsTC MANE Select ENSP00000369129.3:p.Ser2861=
ENST00000379802.7:c.8581_8582delinsTC ENSP00000369129.3:p.Ser2861=
ENST00000418664.2:c.6784_6785delinsTC ENSP00000396591.2:p.Ser2262=
NM_001008844.1:c.6784_6785delinsTC NP_001008844.1:p.Ser2262=
NM_004415.2:c.8581_8582delinsTC , LRG_423t1:c.8581_8582delinsTC NP_004406.2:p.Ser2861=
XM_011514323.1:c.7252_7253delinsTC XP_011512625.1:p.Ser2418=
NM_001008844.2:c.6784_6785delinsTC NP_001008844.1:p.Ser2262=
NM_001319034.1:c.7252_7253delinsTC NP_001305963.1:p.Ser2418=
NM_004415.3:c.8581_8582delinsTC NP_004406.2:p.Ser2861=
NM_004415.4:c.8581_8582delinsTC MANE Select NP_004406.2:p.Ser2861=
NM_001008844.3:c.6784_6785delinsTC NP_001008844.1:p.Ser2262=
NM_001319034.2:c.7252_7253delinsTC NP_001305963.1:p.Ser2418=