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WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled: We are investigating the periodic unresponsiveness in the Registry. Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries. This temporarily affects the API and the UI.
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.186284119T= , CM000666.2:g.186284119T=
GRCh38
NC_000004.11:g.187205273T= , CM000666.1:g.187205273T=
GRCh37
NC_000004.10:g.187442267T=
NCBI36
NG_008051.1:g.23156T= , LRG_583:g.23156T=
Transcript Alleles
HGVS
Amino-acid change
ENST00000403665.7:c.1163T=
MANE Select
ENSP00000384957.2:p.Ile388=
ENST00000264692.8:c.1001T=
ENSP00000264692.5:p.Ile334=
ENST00000403665.6:c.1163T=
ENSP00000384957.2:p.Ile388=
NM_000128.3:c.1163T= , LRG_583t1:c.1163T=
NP_000119.1:p.Ile388=
XM_005262821.2:c.1166T=
XP_005262878.1:p.Ile389=
XM_005262822.2:c.1166T=
XP_005262879.1:p.Ile389=
XM_005262823.2:c.896T=
XP_005262880.1:p.Ile299=
XM_005262824.1:c.1166T=
XP_005262881.1:p.Ile389=
XM_006714137.1:c.1118T=
XP_006714200.1:p.Ile373=
XR_938706.1:n.1571T=
XR_938707.1:n.1571T=
XM_005262821.4:c.1166T=
XP_005262878.1:p.Ile389=
XM_005262822.4:c.1166T=
XP_005262879.1:p.Ile389=
XM_005262823.4:c.896T=
XP_005262880.1:p.Ile299=
XM_006714137.3:c.1118T=
XP_006714200.1:p.Ile373=
XM_017007884.2:c.*2135T=
XP_016863373.1:n.*2135T=
XM_017007885.2:c.*31T=
XP_016863374.1:n.*31T=
XR_001741172.2:n.1637T=
NM_000128.4:c.1163T=
MANE Select
NP_000119.1:p.Ile388=