Canonical Allele Identifier: CA2032423439
Gene: ADAMTS20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.43536193A>T , CM000674.2:g.43536193A>T GRCh38
NC_000012.11:g.43929996A>T , CM000674.1:g.43929996A>T GRCh37
NC_000012.10:g.42216263A>T NCBI36
NG_028228.1:g.20729T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389420.8:c.454-3998T>A MANE Select ENSP00000374071.3:n.454-3998T>A
ENST00000389420.7:c.454-3998T>A ENSP00000374071.3:n.454-3998T>A
ENST00000395541.3:c.456-4000T>A ENSP00000378911.3:n.456-4000T>A
ENST00000553158.5:c.454-3998T>A ENSP00000448341.1:n.454-3998T>A
NM_025003.3:c.454-3998T>A NP_079279.3:n.454-3998T>A
XM_011538754.1:c.454-3998T>A XP_011537056.1:n.454-3998T>A
NM_025003.4:c.454-3998T>A NP_079279.3:n.454-3998T>A
XM_011538754.2:c.454-3998T>A XP_011537056.1:n.454-3998T>A
NM_025003.5:c.454-3998T>A MANE Select NP_079279.3:n.454-3998T>A