Canonical Allele Identifier: CA362690254

Gene: DSP

Linked Data

• dbSNP Id: rs1759518544
• gnomAD v4: 6-7583444-C-T
• MyVariant Identifiers: chr6:g.7583677C>T (hg19) ; chr6:g.7583444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583444C>T , CM000668.2:g.7583444C>T	GRCh38
NC_000006.11:g.7583677C>T , CM000668.1:g.7583677C>T	GRCh37
NC_000006.10:g.7528676C>T	NCBI36
NG_008803.1:g.46808C>T , LRG_423:g.46808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4853C>T	ENSP00000518230.1:p.Pro1618Leu
ENST00000379802.8:c.6182C>T MANE Select	ENSP00000369129.3:p.Pro2061Leu
ENST00000379802.7:c.6182C>T	ENSP00000369129.3:p.Pro2061Leu
ENST00000418664.2:c.4385C>T	ENSP00000396591.2:p.Pro1462Leu
NM_001008844.1:c.4385C>T	NP_001008844.1:p.Pro1462Leu
NM_004415.2:c.6182C>T , LRG_423t1:c.6182C>T	NP_004406.2:p.Pro2061Leu
XM_011514323.1:c.4853C>T	XP_011512625.1:p.Pro1618Leu
NM_001008844.2:c.4385C>T	NP_001008844.1:p.Pro1462Leu
NM_001319034.1:c.4853C>T	NP_001305963.1:p.Pro1618Leu
NM_004415.3:c.6182C>T	NP_004406.2:p.Pro2061Leu
NM_004415.4:c.6182C>T MANE Select	NP_004406.2:p.Pro2061Leu
NM_001008844.3:c.4385C>T	NP_001008844.1:p.Pro1462Leu
NM_001319034.2:c.4853C>T	NP_001305963.1:p.Pro1618Leu