Canonical Allele Identifier: CA2671937214

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686269-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686269A>G , CM000666.2:g.121686269A>G	GRCh38
NC_000004.11:g.122607424A>G , CM000666.1:g.122607424A>G	GRCh37
NC_000004.10:g.122826874A>G	NCBI36
NG_032042.1:g.15724T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+19T>C MANE Select	ENSP00000296511.5:n.94+19T>C
ENST00000296511.9:c.94+19T>C	ENSP00000296511.5:n.94+19T>C
ENST00000501272.6:c.10-2792T>C	ENSP00000424106.1:n.10-2792T>C
ENST00000506395.5:c.94+19T>C	ENSP00000421421.1:n.94+19T>C
ENST00000509016.5:n.215+19T>C
ENST00000511552.5:n.480+19T>C
ENST00000513428.5:n.259+19T>C
ENST00000513523.1:n.262+19T>C
ENST00000513728.1:c.94+19T>C	ENSP00000427135.1:n.94+19T>C
ENST00000515017.5:c.94+19T>C	ENSP00000424199.1:n.94+19T>C
NM_001154.3:c.94+19T>C	NP_001145.1:n.94+19T>C
XM_017008141.2:c.94+19T>C	XP_016863630.1:n.94+19T>C
NM_001154.4:c.94+19T>C MANE Select	NP_001145.1:n.94+19T>C