Canonical Allele Identifier: CA2673314757

Gene: ANKH

Linked Data

• gnomAD v4: 5-14871521-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871521G>A , CM000667.2:g.14871521G>A	GRCh38
NC_000005.9:g.14871630G>A , CM000667.1:g.14871630G>A	GRCh37
NC_000005.8:g.14924630G>A	NCBI36
NG_008273.1:g.5258C>T
NG_008273.2:g.5265C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.-74C>T MANE Select	ENSP00000284268.6:n.-74C>T
ENST00000284268.6:c.-74C>T	ENSP00000284268.6:n.-74C>T
ENST00000505140.1:c.-74C>T	ENSP00000426332.1:n.-74C>T
NM_054027.4:c.-74C>T	NP_473368.1:n.-74C>T
XM_011514067.1:c.-74C>T	XP_011512369.1:n.-74C>T
NM_054027.5:c.-74C>T	NP_473368.1:n.-74C>T
NM_054027.6:c.-74C>T MANE Select	NP_473368.1:n.-74C>T