Canonical Allele Identifier: CA4363121

Gene: KPNA7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99181880C>T , CM000669.2:g.99181880C>T	GRCh38
NC_000007.13:g.98779503C>T , CM000669.1:g.98779503C>T	GRCh37
NC_000007.12:g.98617439C>T	NCBI36
NG_051213.1:g.42538G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001145715.3:c.1317+3G>A MANE Select	NP_001139187.1:n.1317+3G>A
ENST00000327442.7:c.1317+3G>A MANE Select	ENSP00000330878.6:n.1317+3G>A
NM_001145715.1:c.1317+3G>A	NP_001139187.1:n.1317+3G>A
NM_001145715.2:c.1317+3G>A	NP_001139187.1:n.1317+3G>A
ENST00000327442.6:c.1317+3G>A	ENSP00000330878.6:n.1317+3G>A
ENST00000681060.1:c.1317+3G>A	ENSP00000506489.1:n.1317+3G>A
XM_006715987.2:c.1317+3G>A	XP_006716050.1:n.1317+3G>A
XM_011516215.1:c.1398+3G>A	XP_011514517.1:n.1398+3G>A
XM_011516215.2:c.1398+3G>A	XP_011514517.1:n.1398+3G>A
XM_011516216.1:c.1386+3G>A	XP_011514518.1:n.1386+3G>A
XM_011516217.1:c.1365+3G>A	XP_011514519.1:n.1365+3G>A
XM_011516218.1:c.1317+3G>A	XP_011514520.1:n.1317+3G>A
XM_011516219.1:c.1317+3G>A	XP_011514521.1:n.1317+3G>A
XM_011516220.1:c.1317+3G>A	XP_011514522.1:n.1317+3G>A
XM_011516221.1:c.1029+3G>A	XP_011514523.1:n.1029+3G>A
XM_017012208.1:c.1398+3G>A	XP_016867697.1:n.1398+3G>A
XM_017012209.1:c.1386+3G>A	XP_016867698.1:n.1386+3G>A
XM_017012210.1:c.1365+3G>A	XP_016867699.1:n.1365+3G>A
XM_017012211.1:c.1398+3G>A	XP_016867700.1:n.1398+3G>A
XM_017012212.1:c.1317+3G>A	XP_016867701.1:n.1317+3G>A
XM_017012213.1:c.1317+3G>A	XP_016867702.1:n.1317+3G>A
XM_017012214.1:c.1317+3G>A	XP_016867703.1:n.1317+3G>A
XM_017012215.1:c.1215+3049G>A	XP_016867704.1:n.1215+3049G>A
XM_017012216.1:c.1029+3G>A	XP_016867705.1:n.1029+3G>A