Canonical Allele Identifier: CA362674213

Gene: DSP

Linked Data

• ClinVar Variation Id: 2943617
• ClinVar RCV Id: RCV003803175
• MyVariant Identifiers: chr6:g.7565643C>T (hg19) ; chr6:g.7565410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565410C>T , CM000668.2:g.7565410C>T	GRCh38
NC_000006.11:g.7565643C>T , CM000668.1:g.7565643C>T	GRCh37
NC_000006.10:g.7510642C>T	NCBI36
NG_008803.1:g.28774C>T , LRG_423:g.28774C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.829C>T	ENSP00000518230.1:p.Gln277Ter
ENST00000682228.1:n.153C>T
ENST00000379802.8:c.829C>T MANE Select	ENSP00000369129.3:p.Gln277Ter
ENST00000379802.7:c.829C>T	ENSP00000369129.3:p.Gln277Ter
ENST00000418664.2:c.829C>T	ENSP00000396591.2:p.Gln277Ter
ENST00000506617.1:n.347C>T
NM_001008844.1:c.829C>T	NP_001008844.1:p.Gln277Ter
NM_004415.2:c.829C>T , LRG_423t1:c.829C>T	NP_004406.2:p.Gln277Ter
XM_011514323.1:c.829C>T	XP_011512625.1:p.Gln277Ter
NM_001008844.2:c.829C>T	NP_001008844.1:p.Gln277Ter
NM_001319034.1:c.829C>T	NP_001305963.1:p.Gln277Ter
NM_004415.3:c.829C>T	NP_004406.2:p.Gln277Ter
NM_004415.4:c.829C>T MANE Select	NP_004406.2:p.Gln277Ter
NM_001008844.3:c.829C>T	NP_001008844.1:p.Gln277Ter
NM_001319034.2:c.829C>T	NP_001305963.1:p.Gln277Ter