Canonical Allele Identifier: CA362694622
Gene: DSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585447T>A , CM000668.2:g.7585447T>A GRCh38
NC_000006.11:g.7585680T>A , CM000668.1:g.7585680T>A GRCh37
NC_000006.10:g.7530679T>A NCBI36
NG_008803.1:g.48811T>A , LRG_423:g.48811T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6856T>A ENSP00000518230.1:p.Phe2286Ile
ENST00000379802.8:c.8185T>A MANE Select ENSP00000369129.3:p.Phe2729Ile
ENST00000379802.7:c.8185T>A ENSP00000369129.3:p.Phe2729Ile
ENST00000418664.2:c.6388T>A ENSP00000396591.2:p.Phe2130Ile
NM_001008844.1:c.6388T>A NP_001008844.1:p.Phe2130Ile
NM_004415.2:c.8185T>A , LRG_423t1:c.8185T>A NP_004406.2:p.Phe2729Ile
XM_011514323.1:c.6856T>A XP_011512625.1:p.Phe2286Ile
NM_001008844.2:c.6388T>A NP_001008844.1:p.Phe2130Ile
NM_001319034.1:c.6856T>A NP_001305963.1:p.Phe2286Ile
NM_004415.3:c.8185T>A NP_004406.2:p.Phe2729Ile
NM_004415.4:c.8185T>A MANE Select NP_004406.2:p.Phe2729Ile
NM_001008844.3:c.6388T>A NP_001008844.1:p.Phe2130Ile
NM_001319034.2:c.6856T>A NP_001305963.1:p.Phe2286Ile