Canonical Allele Identifier: CA1528949140

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871524_14871526delinsCGA , CM000667.2:g.14871524_14871526delinsCGA	GRCh38
NC_000005.9:g.14871633_14871635delinsCGA , CM000667.1:g.14871633_14871635delinsCGA	GRCh37
NC_000005.8:g.14924633_14924635delinsCGA	NCBI36
NG_008273.1:g.5253_5255delinsTCG
NG_008273.2:g.5260_5262delinsTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.-79_-77delinsTCG MANE Select	ENSP00000284268.6:n.-79_-77delinsTCG
ENST00000284268.6:c.-79_-77delinsTCG	ENSP00000284268.6:n.-79_-77delinsTCG
ENST00000505140.1:c.-79_-77delinsTCG	ENSP00000426332.1:n.-79_-77delinsTCG
NM_054027.4:c.-79_-77delinsTCG	NP_473368.1:n.-79_-77delinsTCG
XM_011514067.1:c.-79_-77delinsTCG	XP_011512369.1:n.-79_-77delinsTCG
NM_054027.5:c.-79_-77delinsTCG	NP_473368.1:n.-79_-77delinsTCG
NM_054027.6:c.-79_-77delinsTCG MANE Select	NP_473368.1:n.-79_-77delinsTCG