Canonical Allele Identifier: CA805671718

Gene: ANXA6

Linked Data

• dbSNP Id: rs1434848601
• gnomAD v4: 5-151101114-C-G
• MyVariant Identifiers: chr5:g.150480675C>G (hg19) ; chr5:g.151101114C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101114C>G , CM000667.2:g.151101114C>G	GRCh38
NC_000005.9:g.150480675C>G , CM000667.1:g.150480675C>G	GRCh37
NC_000005.8:g.150460868C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354546.10:c.*334G>C MANE Select	ENSP00000346550.5:n.*334G>C
ENST00000354546.9:c.*334G>C	ENSP00000346550.5:n.*334G>C
ENST00000377751.9:c.*334G>C	ENSP00000366980.5:n.*334G>C
ENST00000522664.5:c.201-152G>C
ENST00000523714.5:c.*334G>C	ENSP00000430517.1:n.*334G>C
NM_001155.4:c.*334G>C	NP_001146.2:n.*334G>C
NM_001193544.1:c.*334G>C	NP_001180473.1:n.*334G>C
XM_005268432.3:c.*334G>C	XP_005268489.1:n.*334G>C
NM_001363114.1:c.*334G>C	NP_001350043.1:n.*334G>C
NM_001155.5:c.*334G>C MANE Select	NP_001146.2:n.*334G>C
NM_001193544.2:c.*334G>C	NP_001180473.1:n.*334G>C
NM_001363114.2:c.*334G>C	NP_001350043.1:n.*334G>C