Canonical Allele Identifier: CA104728814
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs980762765

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693640A>G , CM000666.2:g.121693640A>G GRCh38
NC_000004.11:g.122614795A>G , CM000666.1:g.122614795A>G GRCh37
NC_000004.10:g.122834245A>G NCBI36
NG_032042.1:g.8353T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+2941T>C MANE Select ENSP00000296511.5:n.9+2941T>C
ENST00000296511.9:c.9+2941T>C ENSP00000296511.5:n.9+2941T>C
ENST00000501272.6:c.9+2941T>C ENSP00000424106.1:n.9+2941T>C
ENST00000506395.5:c.9+2941T>C ENSP00000421421.1:n.9+2941T>C
ENST00000509016.5:n.130+3223T>C
ENST00000511552.5:n.395+2941T>C
ENST00000513428.5:n.174+2941T>C
ENST00000513523.1:n.177+2941T>C
ENST00000513728.1:c.9+2941T>C ENSP00000427135.1:n.9+2941T>C
ENST00000515017.5:c.9+2941T>C ENSP00000424199.1:n.9+2941T>C
NM_001154.3:c.9+2941T>C NP_001145.1:n.9+2941T>C
XM_017008141.2:c.9+2941T>C XP_016863630.1:n.9+2941T>C
NM_001154.4:c.9+2941T>C MANE Select NP_001145.1:n.9+2941T>C