Canonical Allele Identifier: CA3208918
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs375741936
gnomAD v2: 5-14716823-G-A
gnomAD v4: 5-14716714-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716714G>A , CM000667.2:g.14716714G>A GRCh38
NC_000005.9:g.14716823G>A , CM000667.1:g.14716823G>A GRCh37
NC_000005.8:g.14769823G>A NCBI36
NG_008273.1:g.160065C>T
NG_008273.2:g.160072C>T
NG_051625.1:g.60921G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1133C>T MANE Select ENSP00000284268.6:p.Pro378Leu
ENST00000284268.6:c.1133C>T ENSP00000284268.6:p.Pro378Leu
ENST00000502585.1:n.375C>T
NM_054027.4:c.1133C>T NP_473368.1:p.Pro378Leu
NM_054027.5:c.1133C>T NP_473368.1:p.Pro378Leu
XM_017009644.2:c.1049C>T XP_016865133.1:p.Pro350Leu
NM_054027.6:c.1133C>T MANE Select NP_473368.1:p.Pro378Leu