Canonical Allele Identifier: CA050189

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7584851T>C , CM000668.2:g.7584851T>C	GRCh38
NC_000006.11:g.7585084T>C , CM000668.1:g.7585084T>C	GRCh37
NC_000006.10:g.7530083T>C	NCBI36
NG_008803.1:g.48215T>C , LRG_423:g.48215T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.7589T>C MANE Select	NP_004406.2:p.Ile2530Thr
ENST00000379802.8:c.7589T>C MANE Select	ENSP00000369129.3:p.Ile2530Thr
NM_001008844.1:c.5792T>C	NP_001008844.1:p.Ile1931Thr
NM_001008844.2:c.5792T>C	NP_001008844.1:p.Ile1931Thr
NM_001008844.3:c.5792T>C	NP_001008844.1:p.Ile1931Thr
NM_001319034.1:c.6260T>C	NP_001305963.1:p.Ile2087Thr
NM_001319034.2:c.6260T>C	NP_001305963.1:p.Ile2087Thr
NM_004415.2:c.7589T>C , LRG_423t1:c.7589T>C	NP_004406.2:p.Ile2530Thr
NM_004415.3:c.7589T>C	NP_004406.2:p.Ile2530Thr
ENST00000379802.7:c.7589T>C	ENSP00000369129.3:p.Ile2530Thr
ENST00000418664.2:c.5792T>C	ENSP00000396591.2:p.Ile1931Thr
ENST00000710359.1:c.6260T>C	ENSP00000518230.1:p.Ile2087Thr
XM_011514323.1:c.6260T>C	XP_011512625.1:p.Ile2087Thr