Canonical Allele Identifier: CA358037461

Gene: ANXA5

Linked Data

• ClinVar Variation Id: 2617462
• ClinVar RCV Id: RCV004359271
• gnomAD v4: 4-121686354-T-C
• MyVariant Identifiers: chr4:g.122607509T>C (hg19) ; chr4:g.121686354T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686354T>C , CM000666.2:g.121686354T>C	GRCh38
NC_000004.11:g.122607509T>C , CM000666.1:g.122607509T>C	GRCh37
NC_000004.10:g.122826959T>C	NCBI36
NG_032042.1:g.15639A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.28A>G MANE Select	ENSP00000296511.5:p.Thr10Ala
ENST00000296511.9:c.28A>G	ENSP00000296511.5:p.Thr10Ala
ENST00000501272.6:c.10-2877A>G	ENSP00000424106.1:n.10-2877A>G
ENST00000506395.5:c.28A>G	ENSP00000421421.1:p.Thr10Ala
ENST00000509016.5:n.149A>G
ENST00000511552.5:n.414A>G
ENST00000513428.5:n.193A>G
ENST00000513523.1:n.196A>G
ENST00000513728.1:c.28A>G	ENSP00000427135.1:p.Thr10Ala
ENST00000515017.5:c.28A>G	ENSP00000424199.1:p.Thr10Ala
NM_001154.3:c.28A>G	NP_001145.1:p.Thr10Ala
XM_017008141.2:c.28A>G	XP_016863630.1:p.Thr10Ala
NM_001154.4:c.28A>G MANE Select	NP_001145.1:p.Thr10Ala