Canonical Allele Identifier: CA2676216400
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157471610G>T , CM000667.2:g.157471610G>T GRCh38
NC_000005.9:g.156898618G>T , CM000667.1:g.156898618G>T GRCh37
NC_000005.8:g.156831196G>T NCBI36
NG_016626.1:g.16592G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311946.8:c.426-47G>T (NIPAL4) MANE Select ENSP00000311687.8:n.426-47G>T
ENST00000435489.7:c.369-47G>T (NIPAL4) ENSP00000406456.3:n.369-47G>T
ENST00000311946.7:c.612-47G>T (NIPAL4) ENSP00000311687.7:n.612-47G>T
ENST00000435489.6:c.555-47G>T (NIPAL4) ENSP00000406456.2:n.555-47G>T
ENST00000517951.5:c.*1741+16655C>A (ADAM19) ENSP00000428376.1:n.*1741+16655C>A
ENST00000519150.1:c.524-47G>T (NIPAL4) ENSP00000430810.1:n.524-47G>T
NM_001099287.1:c.612-47G>T (NIPAL4) NP_001092757.1:n.612-47G>T
NM_001172292.1:c.555-47G>T (NIPAL4) NP_001165763.1:n.555-47G>T
XM_011534552.1:c.117-47G>T (NIPAL4) XP_011532854.1:n.117-47G>T
XM_024446043.1:c.-88-47G>T (NIPAL4) XP_024301811.1:n.-88-47G>T
NM_001099287.2:c.426-47G>T (NIPAL4) MANE Select NP_001092757.2:n.426-47G>T
Search 100 bp 5'
Search 100 bp 3'