Canonical Allele Identifier: CA1591241170

Gene: ANXA6

Linked Data

• dbSNP Id: rs1581969984

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101126A>G , CM000667.2:g.151101126A>G	GRCh38
NC_000005.9:g.150480687A>G , CM000667.1:g.150480687A>G	GRCh37
NC_000005.8:g.150460880A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700367.1:c.*322T>C	ENSP00000514965.1:n.*322T>C
ENST00000354546.10:c.*322T>C MANE Select	ENSP00000346550.5:n.*322T>C
ENST00000354546.9:c.*322T>C	ENSP00000346550.5:n.*322T>C
ENST00000377751.9:c.*322T>C	ENSP00000366980.5:n.*322T>C
ENST00000522664.5:c.201-164T>C
ENST00000523714.5:c.*322T>C	ENSP00000430517.1:n.*322T>C
NM_001155.4:c.*322T>C	NP_001146.2:n.*322T>C
NM_001193544.1:c.*322T>C	NP_001180473.1:n.*322T>C
XM_005268432.3:c.*322T>C	XP_005268489.1:n.*322T>C
NM_001363114.1:c.*322T>C	NP_001350043.1:n.*322T>C
NM_001155.5:c.*322T>C MANE Select	NP_001146.2:n.*322T>C
NM_001193544.2:c.*322T>C	NP_001180473.1:n.*322T>C
NM_001363114.2:c.*322T>C	NP_001350043.1:n.*322T>C