Canonical Allele Identifier: CA104731712

Gene: ANXA5

Linked Data

• dbSNP Id: rs533223702
• gnomAD v3: 4-121696842-C-T
• gnomAD v4: 4-121696842-C-T
• MyVariant Identifiers: chr4:g.122617997C>T (hg19) ; chr4:g.121696842C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696842C>T , CM000666.2:g.121696842C>T	GRCh38
NC_000004.11:g.122617997C>T , CM000666.1:g.122617997C>T	GRCh37
NC_000004.10:g.122837447C>T	NCBI36
NG_032042.1:g.5151G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-36+21G>A MANE Select	ENSP00000296511.5:n.-36+21G>A
ENST00000296511.9:c.-36+21G>A	ENSP00000296511.5:n.-36+21G>A
ENST00000501272.6:c.-36+21G>A	ENSP00000424106.1:n.-36+21G>A
ENST00000506395.5:c.-36+21G>A	ENSP00000421421.1:n.-36+21G>A
ENST00000509016.5:n.130+21G>A
ENST00000511552.5:n.134G>A
ENST00000513428.5:n.130+21G>A
ENST00000513523.1:n.133+21G>A
ENST00000513728.1:c.-36+21G>A	ENSP00000427135.1:n.-36+21G>A
ENST00000515017.5:c.-36+21G>A	ENSP00000424199.1:n.-36+21G>A
NM_001154.3:c.-36+21G>A	NP_001145.1:n.-36+21G>A
XM_017008141.2:c.-36+21G>A	XP_016863630.1:n.-36+21G>A
NM_001154.4:c.-36+21G>A MANE Select	NP_001145.1:n.-36+21G>A