Canonical Allele Identifier: CA104722818

Gene: ANXA5

Linked Data

• dbSNP Id: rs893015131
• MyVariant Identifiers: chr4:g.122606720G>A (hg19) ; chr4:g.121685565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685565G>A , CM000666.2:g.121685565G>A	GRCh38
NC_000004.11:g.122606720G>A , CM000666.1:g.122606720G>A	GRCh37
NC_000004.10:g.122826170G>A	NCBI36
NG_032042.1:g.16428C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+723C>T MANE Select	ENSP00000296511.5:n.94+723C>T
ENST00000296511.9:c.94+723C>T	ENSP00000296511.5:n.94+723C>T
ENST00000501272.6:c.10-2088C>T	ENSP00000424106.1:n.10-2088C>T
ENST00000506395.5:c.94+723C>T	ENSP00000421421.1:n.94+723C>T
ENST00000509016.5:n.215+723C>T
ENST00000511552.5:n.480+723C>T
ENST00000513428.5:n.259+723C>T
ENST00000513523.1:n.262+723C>T
ENST00000513728.1:c.94+723C>T	ENSP00000427135.1:n.94+723C>T
ENST00000515017.5:c.94+723C>T	ENSP00000424199.1:n.94+723C>T
NM_001154.3:c.94+723C>T	NP_001145.1:n.94+723C>T
XM_017008141.2:c.94+723C>T	XP_016863630.1:n.94+723C>T
NM_001154.4:c.94+723C>T MANE Select	NP_001145.1:n.94+723C>T