Canonical Allele Identifier: CA1528949220

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871585_14871607delinsGGCGGCGGCTCCTCCTCGCGGCT , CM000667.2:g.14871585_14871607delinsGGCGGCGGCTCCTCCTCGCGGCT	GRCh38
NC_000005.9:g.14871694_14871716delinsGGCGGCGGCTCCTCCTCGCGGCT , CM000667.1:g.14871694_14871716delinsGGCGGCGGCTCCTCCTCGCGGCT	GRCh37
NC_000005.8:g.14924694_14924716delinsGGCGGCGGCTCCTCCTCGCGGCT	NCBI36
NG_008273.1:g.5172_5194delinsAGCCGCGAGGAGGAGCCGCCGCC
NG_008273.2:g.5179_5201delinsAGCCGCGAGGAGGAGCCGCCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC MANE Select	ENSP00000284268.6:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC
ENST00000284268.6:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC	ENSP00000284268.6:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC
ENST00000505140.1:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC	ENSP00000426332.1:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC
NM_054027.4:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC	NP_473368.1:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC
XM_011514067.1:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC	XP_011512369.1:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC
NM_054027.5:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC	NP_473368.1:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC
NM_054027.6:c.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC MANE Select	NP_473368.1:n.-160_-138delinsAGCCGCGAGGAGGAGCCGCCGCC