Canonical Allele Identifier: CA2578273171

Linked Data

gnomAD v4: 5-14711178-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14711178G>T , CM000667.2:g.14711178G>T GRCh38
NC_000005.9:g.14711287G>T , CM000667.1:g.14711287G>T GRCh37
NC_000005.8:g.14764287G>T NCBI36
NG_008273.1:g.165601C>A
NG_008273.2:g.165608C>A
NG_051625.1:g.55385G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.*19C>A (ANKH) MANE Select ENSP00000284268.6:n.*19C>A
ENST00000284268.6:c.*19C>A (ANKH) ENSP00000284268.6:n.*19C>A
ENST00000502585.1:n.740C>A (ANKH)
NM_054027.4:c.*19C>A (ANKH) NP_473368.1:n.*19C>A
XM_011514151.1:c.*47-1544G>T (OTULIN) XP_011512453.1:n.*47-1544G>T
NM_054027.5:c.*19C>A (ANKH) NP_473368.1:n.*19C>A
XM_011514151.2:c.*47-1544G>T (OTULIN) XP_011512453.1:n.*47-1544G>T
XM_017009644.2:c.*19C>A (ANKH) XP_016865133.1:n.*19C>A
NM_054027.6:c.*19C>A (ANKH) MANE Select NP_473368.1:n.*19C>A