Canonical Allele Identifier: CA1608620297

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7567233_7567236delinsGCTT , CM000668.2:g.7567233_7567236delinsGCTT	GRCh38
NC_000006.11:g.7567466_7567469delinsGCTT , CM000668.1:g.7567466_7567469delinsGCTT	GRCh37
NC_000006.10:g.7512465_7512468delinsGCTT	NCBI36
NG_008803.1:g.30597_30600delinsGCTT , LRG_423:g.30597_30600delinsGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1045-121_1045-118delinsGCTT	ENSP00000518230.1:n.1045-121_1045-118delinsGCTT
ENST00000682228.1:n.369-121_369-118delinsGCTT
ENST00000379802.8:c.1045-121_1045-118delinsGCTT MANE Select	ENSP00000369129.3:n.1045-121_1045-118delinsGCTT
ENST00000379802.7:c.1045-121_1045-118delinsGCTT	ENSP00000369129.3:n.1045-121_1045-118delinsGCTT
ENST00000418664.2:c.1045-121_1045-118delinsGCTT	ENSP00000396591.2:n.1045-121_1045-118delinsGCTT
NM_001008844.1:c.1045-121_1045-118delinsGCTT	NP_001008844.1:n.1045-121_1045-118delinsGCTT
NM_004415.2:c.1045-121_1045-118delinsGCTT , LRG_423t1:c.1045-121_1045-118delinsGCTT	NP_004406.2:n.1045-121_1045-118delinsGCTT
XM_011514323.1:c.1045-121_1045-118delinsGCTT	XP_011512625.1:n.1045-121_1045-118delinsGCTT
NM_001008844.2:c.1045-121_1045-118delinsGCTT	NP_001008844.1:n.1045-121_1045-118delinsGCTT
NM_001319034.1:c.1045-121_1045-118delinsGCTT	NP_001305963.1:n.1045-121_1045-118delinsGCTT
NM_004415.3:c.1045-121_1045-118delinsGCTT	NP_004406.2:n.1045-121_1045-118delinsGCTT
NM_004415.4:c.1045-121_1045-118delinsGCTT MANE Select	NP_004406.2:n.1045-121_1045-118delinsGCTT
NM_001008844.3:c.1045-121_1045-118delinsGCTT	NP_001008844.1:n.1045-121_1045-118delinsGCTT
NM_001319034.2:c.1045-121_1045-118delinsGCTT	NP_001305963.1:n.1045-121_1045-118delinsGCTT