Canonical Allele Identifier: CA1608615389
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585711_7585719delinsTACAACATG , CM000668.2:g.7585711_7585719delinsTACAACATG GRCh38
NC_000006.11:g.7585944_7585952delinsTACAACATG , CM000668.1:g.7585944_7585952delinsTACAACATG GRCh37
NC_000006.10:g.7530943_7530951delinsTACAACATG NCBI36
NG_008803.1:g.49075_49083delinsTACAACATG , LRG_423:g.49075_49083delinsTACAACATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.7120_7128delinsTACAACATG ENSP00000518230.1:p.Tyr2374=
ENST00000379802.8:c.8449_8457delinsTACAACATG MANE Select ENSP00000369129.3:p.Tyr2817=
ENST00000379802.7:c.8449_8457delinsTACAACATG ENSP00000369129.3:p.Tyr2817=
ENST00000418664.2:c.6652_6660delinsTACAACATG ENSP00000396591.2:p.Tyr2218=
NM_001008844.1:c.6652_6660delinsTACAACATG NP_001008844.1:p.Tyr2218=
NM_004415.2:c.8449_8457delinsTACAACATG , LRG_423t1:c.8449_8457delinsTACAACATG NP_004406.2:p.Tyr2817=
XM_011514323.1:c.7120_7128delinsTACAACATG XP_011512625.1:p.Tyr2374=
NM_001008844.2:c.6652_6660delinsTACAACATG NP_001008844.1:p.Tyr2218=
NM_001319034.1:c.7120_7128delinsTACAACATG NP_001305963.1:p.Tyr2374=
NM_004415.3:c.8449_8457delinsTACAACATG NP_004406.2:p.Tyr2817=
NM_004415.4:c.8449_8457delinsTACAACATG MANE Select NP_004406.2:p.Tyr2817=
NM_001008844.3:c.6652_6660delinsTACAACATG NP_001008844.1:p.Tyr2218=
NM_001319034.2:c.7120_7128delinsTACAACATG NP_001305963.1:p.Tyr2374=