Canonical Allele Identifier: CA2676049913

Gene: ANXA6

Linked Data

• gnomAD v4: 5-151101124-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101124G>A , CM000667.2:g.151101124G>A	GRCh38
NC_000005.9:g.150480685G>A , CM000667.1:g.150480685G>A	GRCh37
NC_000005.8:g.150460878G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700367.1:c.*324C>T	ENSP00000514965.1:n.*324C>T
ENST00000354546.10:c.*324C>T MANE Select	ENSP00000346550.5:n.*324C>T
ENST00000354546.9:c.*324C>T	ENSP00000346550.5:n.*324C>T
ENST00000377751.9:c.*324C>T	ENSP00000366980.5:n.*324C>T
ENST00000522664.5:c.201-162C>T
ENST00000523714.5:c.*324C>T	ENSP00000430517.1:n.*324C>T
NM_001155.4:c.*324C>T	NP_001146.2:n.*324C>T
NM_001193544.1:c.*324C>T	NP_001180473.1:n.*324C>T
XM_005268432.3:c.*324C>T	XP_005268489.1:n.*324C>T
NM_001363114.1:c.*324C>T	NP_001350043.1:n.*324C>T
NM_001155.5:c.*324C>T MANE Select	NP_001146.2:n.*324C>T
NM_001193544.2:c.*324C>T	NP_001180473.1:n.*324C>T
NM_001363114.2:c.*324C>T	NP_001350043.1:n.*324C>T