Canonical Allele Identifier: CA362694094

Gene: DSP

Linked Data

• gnomAD v4: 6-7585196-T-G
• MyVariant Identifiers: chr6:g.7585429T>G (hg19) ; chr6:g.7585196T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585196T>G , CM000668.2:g.7585196T>G	GRCh38
NC_000006.11:g.7585429T>G , CM000668.1:g.7585429T>G	GRCh37
NC_000006.10:g.7530428T>G	NCBI36
NG_008803.1:g.48560T>G , LRG_423:g.48560T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6605T>G	ENSP00000518230.1:p.Ile2202Ser
ENST00000379802.8:c.7934T>G MANE Select	ENSP00000369129.3:p.Ile2645Ser
ENST00000379802.7:c.7934T>G	ENSP00000369129.3:p.Ile2645Ser
ENST00000418664.2:c.6137T>G	ENSP00000396591.2:p.Ile2046Ser
NM_001008844.1:c.6137T>G	NP_001008844.1:p.Ile2046Ser
NM_004415.2:c.7934T>G , LRG_423t1:c.7934T>G	NP_004406.2:p.Ile2645Ser
XM_011514323.1:c.6605T>G	XP_011512625.1:p.Ile2202Ser
NM_001008844.2:c.6137T>G	NP_001008844.1:p.Ile2046Ser
NM_001319034.1:c.6605T>G	NP_001305963.1:p.Ile2202Ser
NM_004415.3:c.7934T>G	NP_004406.2:p.Ile2645Ser
NM_004415.4:c.7934T>G MANE Select	NP_004406.2:p.Ile2645Ser
NM_001008844.3:c.6137T>G	NP_001008844.1:p.Ile2046Ser
NM_001319034.2:c.6605T>G	NP_001305963.1:p.Ile2202Ser