Canonical Allele Identifier: CA1489955273
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1725025082

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693644A>T , CM000666.2:g.121693644A>T GRCh38
NC_000004.11:g.122614799A>T , CM000666.1:g.122614799A>T GRCh37
NC_000004.10:g.122834249A>T NCBI36
NG_032042.1:g.8349T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+2937T>A MANE Select ENSP00000296511.5:n.9+2937T>A
ENST00000296511.9:c.9+2937T>A ENSP00000296511.5:n.9+2937T>A
ENST00000501272.6:c.9+2937T>A ENSP00000424106.1:n.9+2937T>A
ENST00000506395.5:c.9+2937T>A ENSP00000421421.1:n.9+2937T>A
ENST00000509016.5:n.130+3219T>A
ENST00000511552.5:n.395+2937T>A
ENST00000513428.5:n.174+2937T>A
ENST00000513523.1:n.177+2937T>A
ENST00000513728.1:c.9+2937T>A ENSP00000427135.1:n.9+2937T>A
ENST00000515017.5:c.9+2937T>A ENSP00000424199.1:n.9+2937T>A
NM_001154.3:c.9+2937T>A NP_001145.1:n.9+2937T>A
XM_017008141.2:c.9+2937T>A XP_016863630.1:n.9+2937T>A
NM_001154.4:c.9+2937T>A MANE Select NP_001145.1:n.9+2937T>A