Canonical Allele Identifier: CA362690019

Gene: DSP

Linked Data

• ClinVar Variation Id: 666381
• ClinVar RCV Id: RCV001368313 ; RCV001701445 ; RCV003532284 ; RCV004002867 ; RCV003307567
• dbSNP Id: rs1759514545
• gnomAD v4: 6-7583335-C-T
• MyVariant Identifiers: chr6:g.7583568C>T (hg19) ; chr6:g.7583335C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583335C>T , CM000668.2:g.7583335C>T	GRCh38
NC_000006.11:g.7583568C>T , CM000668.1:g.7583568C>T	GRCh37
NC_000006.10:g.7528567C>T	NCBI36
NG_008803.1:g.46699C>T , LRG_423:g.46699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4744C>T	ENSP00000518230.1:p.Pro1582Ser
ENST00000379802.8:c.6073C>T MANE Select	ENSP00000369129.3:p.Pro2025Ser
ENST00000379802.7:c.6073C>T	ENSP00000369129.3:p.Pro2025Ser
ENST00000418664.2:c.4276C>T	ENSP00000396591.2:p.Pro1426Ser
NM_001008844.1:c.4276C>T	NP_001008844.1:p.Pro1426Ser
NM_004415.2:c.6073C>T , LRG_423t1:c.6073C>T	NP_004406.2:p.Pro2025Ser
XM_011514323.1:c.4744C>T	XP_011512625.1:p.Pro1582Ser
NM_001008844.2:c.4276C>T	NP_001008844.1:p.Pro1426Ser
NM_001319034.1:c.4744C>T	NP_001305963.1:p.Pro1582Ser
NM_004415.3:c.6073C>T	NP_004406.2:p.Pro2025Ser
NM_004415.4:c.6073C>T MANE Select	NP_004406.2:p.Pro2025Ser
NM_001008844.3:c.4276C>T	NP_001008844.1:p.Pro1426Ser
NM_001319034.2:c.4744C>T	NP_001305963.1:p.Pro1582Ser