Canonical Allele Identifier: CA1082938734

Gene: ANXA6

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151134177A>T , CM000667.2:g.151134177A>T	GRCh38
NC_000005.9:g.150513738A>T , CM000667.1:g.150513738A>T	GRCh37
NC_000005.8:g.150493931A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700367.1:c.546+250T>A	ENSP00000514965.1:n.546+250T>A
ENST00000354546.10:c.546+250T>A MANE Select	ENSP00000346550.5:n.546+250T>A
ENST00000354546.9:c.546+250T>A	ENSP00000346550.5:n.546+250T>A
ENST00000377751.9:c.204+5176T>A	ENSP00000366980.5:n.204+5176T>A
ENST00000517486.5:c.318+4501T>A	ENSP00000428916.1:n.318+4501T>A
ENST00000517677.5:c.366-990T>A	ENSP00000430826.1:n.366-990T>A
ENST00000519644.6:c.262+4557T>A	ENSP00000430663.2:n.262+4557T>A
ENST00000521512.5:c.224+4595T>A	ENSP00000430420.1:n.224+4595T>A
ENST00000523714.5:c.450+250T>A	ENSP00000430517.1:n.450+250T>A
NM_001155.4:c.546+250T>A	NP_001146.2:n.546+250T>A
NM_001193544.1:c.450+250T>A	NP_001180473.1:n.450+250T>A
XM_005268432.3:c.546+250T>A	XP_005268489.1:n.546+250T>A
NM_001363114.1:c.546+250T>A	NP_001350043.1:n.546+250T>A
NM_001155.5:c.546+250T>A MANE Select	NP_001146.2:n.546+250T>A
NM_001193544.2:c.450+250T>A	NP_001180473.1:n.450+250T>A
NM_001363114.2:c.546+250T>A	NP_001350043.1:n.546+250T>A