Canonical Allele Identifier: CA805671734

Gene: ANXA6

Linked Data

• dbSNP Id: rs1246399003
• gnomAD v3: 5-151101140-G-T
• gnomAD v4: 5-151101140-G-T
• MyVariant Identifiers: chr5:g.150480701G>T (hg19) ; chr5:g.151101140G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101140G>T , CM000667.2:g.151101140G>T	GRCh38
NC_000005.9:g.150480701G>T , CM000667.1:g.150480701G>T	GRCh37
NC_000005.8:g.150460894G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700367.1:c.*308C>A	ENSP00000514965.1:n.*308C>A
ENST00000354546.10:c.*308C>A MANE Select	ENSP00000346550.5:n.*308C>A
ENST00000354546.9:c.*308C>A	ENSP00000346550.5:n.*308C>A
ENST00000377751.9:c.*308C>A	ENSP00000366980.5:n.*308C>A
ENST00000522664.5:c.201-178C>A
ENST00000523714.5:c.*308C>A	ENSP00000430517.1:n.*308C>A
NM_001155.4:c.*308C>A	NP_001146.2:n.*308C>A
NM_001193544.1:c.*308C>A	NP_001180473.1:n.*308C>A
XM_005268432.3:c.*308C>A	XP_005268489.1:n.*308C>A
NM_001363114.1:c.*308C>A	NP_001350043.1:n.*308C>A
NM_001155.5:c.*308C>A MANE Select	NP_001146.2:n.*308C>A
NM_001193544.2:c.*308C>A	NP_001180473.1:n.*308C>A
NM_001363114.2:c.*308C>A	NP_001350043.1:n.*308C>A