Canonical Allele Identifier: CA2673310562

Gene: ANKH

Linked Data

• gnomAD v4: 5-14716898-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14716898T>A , CM000667.2:g.14716898T>A	GRCh38
NC_000005.9:g.14717007T>A , CM000667.1:g.14717007T>A	GRCh37
NC_000005.8:g.14770007T>A	NCBI36
NG_008273.1:g.159881A>T
NG_008273.2:g.159888A>T
NG_051625.1:g.61105T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.1012-63A>T MANE Select	ENSP00000284268.6:n.1012-63A>T
ENST00000284268.6:c.1012-63A>T	ENSP00000284268.6:n.1012-63A>T
ENST00000502585.1:n.191A>T
NM_054027.4:c.1012-63A>T	NP_473368.1:n.1012-63A>T
NM_054027.5:c.1012-63A>T	NP_473368.1:n.1012-63A>T
XM_017009644.2:c.928-63A>T	XP_016865133.1:n.928-63A>T
NM_054027.6:c.1012-63A>T MANE Select	NP_473368.1:n.1012-63A>T