Canonical Allele Identifier: CA362690066

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7583590T>C (hg19) ; chr6:g.7583357T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583357T>C , CM000668.2:g.7583357T>C	GRCh38
NC_000006.11:g.7583590T>C , CM000668.1:g.7583590T>C	GRCh37
NC_000006.10:g.7528589T>C	NCBI36
NG_008803.1:g.46721T>C , LRG_423:g.46721T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.4766T>C	ENSP00000518230.1:p.Val1589Ala
ENST00000379802.8:c.6095T>C MANE Select	ENSP00000369129.3:p.Val2032Ala
ENST00000379802.7:c.6095T>C	ENSP00000369129.3:p.Val2032Ala
ENST00000418664.2:c.4298T>C	ENSP00000396591.2:p.Val1433Ala
NM_001008844.1:c.4298T>C	NP_001008844.1:p.Val1433Ala
NM_004415.2:c.6095T>C , LRG_423t1:c.6095T>C	NP_004406.2:p.Val2032Ala
XM_011514323.1:c.4766T>C	XP_011512625.1:p.Val1589Ala
NM_001008844.2:c.4298T>C	NP_001008844.1:p.Val1433Ala
NM_001319034.1:c.4766T>C	NP_001305963.1:p.Val1589Ala
NM_004415.3:c.6095T>C	NP_004406.2:p.Val2032Ala
NM_004415.4:c.6095T>C MANE Select	NP_004406.2:p.Val2032Ala
NM_001008844.3:c.4298T>C	NP_001008844.1:p.Val1433Ala
NM_001319034.2:c.4766T>C	NP_001305963.1:p.Val1589Ala