Canonical Allele Identifier: CA3063058

Gene: ANXA5

Linked Data

• dbSNP Id: rs777804931
• ExAC: 4:122607577 A / G
• gnomAD v2: 4-122607577-A-G
• gnomAD v4: 4-121686422-A-G
• MyVariant Identifiers: chr4:g.122607577A>G (hg19) ; chr4:g.121686422A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686422A>G , CM000666.2:g.121686422A>G	GRCh38
NC_000004.11:g.122607577A>G , CM000666.1:g.122607577A>G	GRCh37
NC_000004.10:g.122827027A>G	NCBI36
NG_032042.1:g.15571T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-50T>C MANE Select	ENSP00000296511.5:n.10-50T>C
ENST00000296511.9:c.10-50T>C	ENSP00000296511.5:n.10-50T>C
ENST00000501272.6:c.10-2945T>C	ENSP00000424106.1:n.10-2945T>C
ENST00000506395.5:c.10-50T>C	ENSP00000421421.1:n.10-50T>C
ENST00000509016.5:n.131-50T>C
ENST00000511552.5:n.396-50T>C
ENST00000513428.5:n.175-50T>C
ENST00000513523.1:n.178-50T>C
ENST00000513728.1:c.10-50T>C	ENSP00000427135.1:n.10-50T>C
ENST00000515017.5:c.10-50T>C	ENSP00000424199.1:n.10-50T>C
NM_001154.3:c.10-50T>C	NP_001145.1:n.10-50T>C
XM_017008141.2:c.10-50T>C	XP_016863630.1:n.10-50T>C
NM_001154.4:c.10-50T>C MANE Select	NP_001145.1:n.10-50T>C