Canonical Allele Identifier: CA1489955207
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693457_121693458delinsTA , CM000666.2:g.121693457_121693458delinsTA GRCh38
NC_000004.11:g.122614612_122614613delinsTA , CM000666.1:g.122614612_122614613delinsTA GRCh37
NC_000004.10:g.122834062_122834063delinsTA NCBI36
NG_032042.1:g.8535_8536delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.9+3123_9+3124delinsTA MANE Select ENSP00000296511.5:n.9+3123_9+3124delinsTA
ENST00000296511.9:c.9+3123_9+3124delinsTA ENSP00000296511.5:n.9+3123_9+3124delinsTA
ENST00000501272.6:c.9+3123_9+3124delinsTA ENSP00000424106.1:n.9+3123_9+3124delinsTA
ENST00000506395.5:c.9+3123_9+3124delinsTA ENSP00000421421.1:n.9+3123_9+3124delinsTA
ENST00000509016.5:n.130+3405_130+3406delinsTA
ENST00000511552.5:n.395+3123_395+3124delinsTA
ENST00000513428.5:n.174+3123_174+3124delinsTA
ENST00000513523.1:n.177+3123_177+3124delinsTA
ENST00000513728.1:c.9+3123_9+3124delinsTA ENSP00000427135.1:n.9+3123_9+3124delinsTA
ENST00000515017.5:c.9+3123_9+3124delinsTA ENSP00000424199.1:n.9+3123_9+3124delinsTA
NM_001154.3:c.9+3123_9+3124delinsTA NP_001145.1:n.9+3123_9+3124delinsTA
XM_017008141.2:c.9+3123_9+3124delinsTA XP_016863630.1:n.9+3123_9+3124delinsTA
NM_001154.4:c.9+3123_9+3124delinsTA MANE Select NP_001145.1:n.9+3123_9+3124delinsTA