Canonical Allele Identifier: CA1085720289

Gene: DSP

Linked Data

• dbSNP Id: rs772041102
• gnomAD v3: 6-7554125-A-ACACACACACACACACACACACACACACACACACACC
• gnomAD v4: 6-7554125-A-ACACACACACACACACACACACACACACACACACACC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7554126_7554127insACACACACACACACACACACACACACACACACACCC , CM000668.2:g.7554126_7554127insACACACACACACACACACACACACACACACACACCC	GRCh38
NC_000006.11:g.7554359_7554360insACACACACACACACACACACACACACACACACACCC , CM000668.1:g.7554359_7554360insACACACACACACACACACACACACACACACACACCC	GRCh37
NC_000006.10:g.7499358_7499359insACACACACACACACACACACACACACACACACACCC	NCBI36
NG_008803.1:g.17490_17491insACACACACACACACACACACACACACACACACACCC , LRG_423:g.17490_17491insACACACACACACACACACACACACACACACACACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683682.2:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	ENSP00000508162.2:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000710359.1:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	ENSP00000518230.1:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000683563.1:n.63-1592_63-1591insACACACACACACACACACACACACACACACACACCC
ENST00000683682.1:c.66-1592_66-1591insACACACACACACACACACACACACACACACACACCC	ENSP00000508162.1:n.66-1592_66-1591insACACACACACACACACACACACA...
ENST00000379802.8:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC MANE Select	ENSP00000369129.3:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000379802.7:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	ENSP00000369129.3:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000418664.2:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	ENSP00000396591.2:n.171-1592_171-1591insACACACACACACACACACACA...
NM_001008844.1:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_001008844.1:n.171-1592_171-1591insACACACACACACACACACACACAC...
NM_004415.2:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC , LRG_423t1:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_004406.2:n.171-1592_171-1591insACACACACACACACACACACACACACA...
XM_011514323.1:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	XP_011512625.1:n.171-1592_171-1591insACACACACACACACACACACACAC...
NM_001008844.2:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_001008844.1:n.171-1592_171-1591insACACACACACACACACACACACAC...
NM_001319034.1:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_001305963.1:n.171-1592_171-1591insACACACACACACACACACACACAC...
NM_004415.3:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_004406.2:n.171-1592_171-1591insACACACACACACACACACACACACACA...
NM_004415.4:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC MANE Select	NP_004406.2:n.171-1592_171-1591insACACACACACACACACACACACACACA...
NM_001008844.3:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_001008844.1:n.171-1592_171-1591insACACACACACACACACACACACAC...
NM_001319034.2:c.171-1592_171-1591insACACACACACACACACACACACACACACACACACCC	NP_001305963.1:n.171-1592_171-1591insACACACACACACACACACACACAC...