Canonical Allele Identifier: CA1608617134

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565404_7565408delinsATCAT , CM000668.2:g.7565404_7565408delinsATCAT	GRCh38
NC_000006.11:g.7565637_7565641delinsATCAT , CM000668.1:g.7565637_7565641delinsATCAT	GRCh37
NC_000006.10:g.7510636_7510640delinsATCAT	NCBI36
NG_008803.1:g.28768_28772delinsATCAT , LRG_423:g.28768_28772delinsATCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.823_827delinsATCAT	ENSP00000518230.1:p.Ile275=
ENST00000682228.1:n.147_151delinsATCAT
ENST00000379802.8:c.823_827delinsATCAT MANE Select	ENSP00000369129.3:p.Ile275=
ENST00000379802.7:c.823_827delinsATCAT	ENSP00000369129.3:p.Ile275=
ENST00000418664.2:c.823_827delinsATCAT	ENSP00000396591.2:p.Ile275=
ENST00000506617.1:n.341_345delinsATCAT
NM_001008844.1:c.823_827delinsATCAT	NP_001008844.1:p.Ile275=
NM_004415.2:c.823_827delinsATCAT , LRG_423t1:c.823_827delinsATCAT	NP_004406.2:p.Ile275=
XM_011514323.1:c.823_827delinsATCAT	XP_011512625.1:p.Ile275=
NM_001008844.2:c.823_827delinsATCAT	NP_001008844.1:p.Ile275=
NM_001319034.1:c.823_827delinsATCAT	NP_001305963.1:p.Ile275=
NM_004415.3:c.823_827delinsATCAT	NP_004406.2:p.Ile275=
NM_004415.4:c.823_827delinsATCAT MANE Select	NP_004406.2:p.Ile275=
NM_001008844.3:c.823_827delinsATCAT	NP_001008844.1:p.Ile275=
NM_001319034.2:c.823_827delinsATCAT	NP_001305963.1:p.Ile275=