Canonical Allele Identifier: CA362690570

Gene: DSP

Linked Data

• gnomAD v4: 6-7583594-T-A
• MyVariant Identifiers: chr6:g.7583827T>A (hg19) ; chr6:g.7583594T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583594T>A , CM000668.2:g.7583594T>A	GRCh38
NC_000006.11:g.7583827T>A , CM000668.1:g.7583827T>A	GRCh37
NC_000006.10:g.7528826T>A	NCBI36
NG_008803.1:g.46958T>A , LRG_423:g.46958T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.5003T>A	ENSP00000518230.1:p.Ile1668Asn
ENST00000379802.8:c.6332T>A MANE Select	ENSP00000369129.3:p.Ile2111Asn
ENST00000379802.7:c.6332T>A	ENSP00000369129.3:p.Ile2111Asn
ENST00000418664.2:c.4535T>A	ENSP00000396591.2:p.Ile1512Asn
NM_001008844.1:c.4535T>A	NP_001008844.1:p.Ile1512Asn
NM_004415.2:c.6332T>A , LRG_423t1:c.6332T>A	NP_004406.2:p.Ile2111Asn
XM_011514323.1:c.5003T>A	XP_011512625.1:p.Ile1668Asn
NM_001008844.2:c.4535T>A	NP_001008844.1:p.Ile1512Asn
NM_001319034.1:c.5003T>A	NP_001305963.1:p.Ile1668Asn
NM_004415.3:c.6332T>A	NP_004406.2:p.Ile2111Asn
NM_004415.4:c.6332T>A MANE Select	NP_004406.2:p.Ile2111Asn
NM_001008844.3:c.4535T>A	NP_001008844.1:p.Ile1512Asn
NM_001319034.2:c.5003T>A	NP_001305963.1:p.Ile1668Asn