Canonical Allele Identifier: CA362676645

Gene: DSP

Linked Data

• ClinVar Variation Id: 534293
• ClinVar RCV Id: RCV000641792 ; RCV001270768
• dbSNP Id: rs1554106853
• gnomAD v4: 6-7568552-T-C
• MyVariant Identifiers: chr6:g.7568785T>C (hg19) ; chr6:g.7568552T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568552T>C , CM000668.2:g.7568552T>C	GRCh38
NC_000006.11:g.7568785T>C , CM000668.1:g.7568785T>C	GRCh37
NC_000006.10:g.7513784T>C	NCBI36
NG_008803.1:g.31916T>C , LRG_423:g.31916T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1382T>C	ENSP00000518230.1:p.Ile461Thr
ENST00000379802.8:c.1382T>C MANE Select	ENSP00000369129.3:p.Ile461Thr
ENST00000379802.7:c.1382T>C	ENSP00000369129.3:p.Ile461Thr
ENST00000418664.2:c.1382T>C	ENSP00000396591.2:p.Ile461Thr
NM_001008844.1:c.1382T>C	NP_001008844.1:p.Ile461Thr
NM_004415.2:c.1382T>C , LRG_423t1:c.1382T>C	NP_004406.2:p.Ile461Thr
XM_011514323.1:c.1382T>C	XP_011512625.1:p.Ile461Thr
NM_001008844.2:c.1382T>C	NP_001008844.1:p.Ile461Thr
NM_001319034.1:c.1382T>C	NP_001305963.1:p.Ile461Thr
NM_004415.3:c.1382T>C	NP_004406.2:p.Ile461Thr
NM_004415.4:c.1382T>C MANE Select	NP_004406.2:p.Ile461Thr
NM_001008844.3:c.1382T>C	NP_001008844.1:p.Ile461Thr
NM_001319034.2:c.1382T>C	NP_001305963.1:p.Ile461Thr