Canonical Allele Identifier: CA1620726339
Gene: ANKS1A HGNC NCBI

Linked Data

dbSNP Id: rs13210323

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35037307A>T , CM000668.2:g.35037307A>T GRCh38
NC_000006.11:g.35005084A>T , CM000668.1:g.35005084A>T GRCh37
NC_000006.10:g.35113062A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360359.5:c.2011-16792A>T MANE Select ENSP00000353518.3:n.2011-16792A>T
ENST00000649117.1:c.2074-16792A>T ENSP00000497393.1:n.2074-16792A>T
ENST00000360359.4:c.2011-16792A>T ENSP00000353518.3:n.2011-16792A>T
NM_015245.2:c.2011-16792A>T NP_056060.2:n.2011-16792A>T
XM_005248964.2:c.2074-16792A>T XP_005249021.1:n.2074-16792A>T
XM_006715036.2:c.2074-16792A>T XP_006715099.1:n.2074-16792A>T
XM_011514431.1:c.2074-16792A>T XP_011512733.1:n.2074-16792A>T
XM_011514432.1:c.2074-16792A>T XP_011512734.1:n.2074-16792A>T
XM_011514433.1:c.2074-16792A>T XP_011512735.1:n.2074-16792A>T
XM_011514434.1:c.2011-16792A>T XP_011512736.1:n.2011-16792A>T
XM_011514435.1:c.2011-16792A>T XP_011512737.1:n.2011-16792A>T
XM_011514436.1:c.1876-16792A>T XP_011512738.1:n.1876-16792A>T
XM_011514437.1:c.388-16792A>T XP_011512739.1:n.388-16792A>T
XM_005248964.3:c.2074-16792A>T XP_005249021.1:n.2074-16792A>T
XM_011514431.3:c.2074-16792A>T XP_011512733.1:n.2074-16792A>T
XM_011514432.3:c.2074-16792A>T XP_011512734.1:n.2074-16792A>T
XM_011514434.3:c.2011-16792A>T XP_011512736.1:n.2011-16792A>T
XM_011514435.3:c.2011-16792A>T XP_011512737.1:n.2011-16792A>T
XM_011514436.3:c.1876-16792A>T XP_011512738.1:n.1876-16792A>T
XM_011514437.3:c.388-16792A>T XP_011512739.1:n.388-16792A>T
XM_017010593.1:c.388-16792A>T XP_016866082.1:n.388-16792A>T
XM_024446383.1:c.2074-16792A>T XP_024302151.1:n.2074-16792A>T
NM_015245.3:c.2011-16792A>T MANE Select NP_056060.2:n.2011-16792A>T