Canonical Allele Identifier: CA2630296216
Gene: ANPEP HGNC NCBI

Linked Data

gnomAD v4: 15-89792576-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792576G>T , CM000677.2:g.89792576G>T GRCh38
NC_000015.9:g.90335807G>T , CM000677.1:g.90335807G>T GRCh37
NC_000015.8:g.88136811G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300060.7:c.2250-14C>A MANE Select ENSP00000300060.6:n.2250-14C>A
ENST00000559874.2:c.2250-14C>A ENSP00000452934.2:n.2250-14C>A
ENST00000560137.2:c.2250-14C>A ENSP00000453413.2:n.2250-14C>A
ENST00000679248.1:c.2250-14C>A ENSP00000502886.1:n.2250-14C>A
ENST00000300060.6:c.2250-14C>A ENSP00000300060.6:n.2250-14C>A
ENST00000558740.1:n.154-14C>A
NM_001150.2:c.2250-14C>A NP_001141.2:n.2250-14C>A
XM_005254892.3:c.2250-14C>A XP_005254949.1:n.2250-14C>A
XM_011521473.1:c.2250-14C>A XP_011519775.1:n.2250-14C>A
XM_005254892.4:c.2250-14C>A XP_005254949.1:n.2250-14C>A
NM_001150.3:c.2250-14C>A MANE Select NP_001141.2:n.2250-14C>A
NM_001381923.1:c.2250-14C>A NP_001368852.1:n.2250-14C>A
NM_001381924.1:c.2250-14C>A NP_001368853.1:n.2250-14C>A
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