Canonical Allele Identifier: CA448716893

Gene: DSP

Linked Data

• ClinVar Variation Id: 1761147
• ClinVar RCV Id: RCV002412372
• MyVariant Identifiers: chr6:g.7585397A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585164A>T , CM000668.2:g.7585164A>T	GRCh38
NC_000006.11:g.7585397A>T , CM000668.1:g.7585397A>T	GRCh37
NC_000006.10:g.7530396A>T	NCBI36
NG_008803.1:g.48528A>T , LRG_423:g.48528A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6573A>T	ENSP00000518230.1:p.Thr2191=
ENST00000379802.8:c.7902A>T MANE Select	ENSP00000369129.3:p.Thr2634=
ENST00000379802.7:c.7902A>T	ENSP00000369129.3:p.Thr2634=
ENST00000418664.2:c.6105A>T	ENSP00000396591.2:p.Thr2035=
NM_001008844.1:c.6105A>T	NP_001008844.1:p.Thr2035=
NM_004415.2:c.7902A>T , LRG_423t1:c.7902A>T	NP_004406.2:p.Thr2634=
XM_011514323.1:c.6573A>T	XP_011512625.1:p.Thr2191=
NM_001008844.2:c.6105A>T	NP_001008844.1:p.Thr2035=
NM_001319034.1:c.6573A>T	NP_001305963.1:p.Thr2191=
NM_004415.3:c.7902A>T	NP_004406.2:p.Thr2634=
NM_004415.4:c.7902A>T MANE Select	NP_004406.2:p.Thr2634=
NM_001008844.3:c.6105A>T	NP_001008844.1:p.Thr2035=
NM_001319034.2:c.6573A>T	NP_001305963.1:p.Thr2191=