Canonical Allele Identifier: CA2664273203

Linked Data

gnomAD v4: 3-8768550-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768555del , CM000665.2:g.8768555del GRCh38
NC_000003.11:g.8810241del , CM000665.1:g.8810241del GRCh37
NC_000003.10:g.8785241del NCBI36
NG_008797.2:g.39746del , LRG_329:g.39746del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.-198del (OXTR) MANE Select ENSP00000324270.2:n.-198del
ENST00000316793.7:c.-198del (OXTR) ENSP00000324270.2:n.-198del
ENST00000431493.1:c.-198del (OXTR) ENSP00000414828.1:n.-198del
ENST00000449615.1:c.-198del (OXTR) ENSP00000389587.1:n.-198del
ENST00000472766.1:n.156-8922del (CAV3)
ENST00000474615.1:n.424del (OXTR)
NM_000916.3:c.-198del (OXTR) NP_000907.2:n.-198del
XM_011533762.1:c.-198del (OXTR) XP_011532064.1:n.-198del
XM_011533763.1:c.-198del (OXTR) XP_011532065.1:n.-198del
NM_001354653.1:c.-198del (OXTR) NP_001341582.1:n.-198del
NM_001354654.1:c.-198del (OXTR) NP_001341583.1:n.-198del
NM_001354655.1:c.-198del (OXTR) NP_001341584.1:n.-198del
NM_001354656.1:c.-198del (OXTR) NP_001341585.1:n.-198del
NM_001354656.2:c.-198del (OXTR) NP_001341585.1:n.-198del
NM_000916.4:c.-198del (OXTR) MANE Select NP_000907.2:n.-198del
NM_001354653.2:c.-198del (OXTR) NP_001341582.1:n.-198del
NM_001354654.2:c.-198del (OXTR) NP_001341583.1:n.-198del
NM_001354655.2:c.-198del (OXTR) NP_001341584.1:n.-198del
NM_001354656.3:c.-198del (OXTR) NP_001341585.1:n.-198del