Canonical Allele Identifier: CA359245549

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14741949G>T (hg19) ; chr5:g.14741840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14741840G>T , CM000667.2:g.14741840G>T	GRCh38
NC_000005.9:g.14741949G>T , CM000667.1:g.14741949G>T	GRCh37
NC_000005.8:g.14794949G>T	NCBI36
NG_008273.1:g.134939C>A
NG_008273.2:g.134946C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000284268.8:c.998C>A MANE Select	ENSP00000284268.6:p.Ala333Asp
ENST00000284268.6:c.998C>A	ENSP00000284268.6:p.Ala333Asp
ENST00000503939.5:n.510C>A
ENST00000515517.1:n.232C>A
NM_054027.4:c.998C>A	NP_473368.1:p.Ala333Asp
XM_011514067.1:c.998C>A	XP_011512369.1:p.Ala333Asp
NM_054027.5:c.998C>A	NP_473368.1:p.Ala333Asp
XM_017009644.2:c.914C>A	XP_016865133.1:p.Ala305Asp
NM_054027.6:c.998C>A MANE Select	NP_473368.1:p.Ala333Asp