Canonical Allele Identifier: CA7727508
Community Standard Title: NM_198525.3(KIF7):c.3842G>T (p.Ser1281Ile)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89628609C>A , CM000677.2:g.89628609C>A GRCh38
NC_000015.9:g.90171840C>A , CM000677.1:g.90171840C>A GRCh37
NC_000015.8:g.87972844C>A NCBI36
NG_030338.1:g.31843G>T

Transcript Alleles

HGVS Amino-acid Change
NM_198525.3:c.3842G>T (KIF7) MANE Select NP_940927.2:p.Ser1281Ile
ENST00000394412.8:c.3842G>T (KIF7) MANE Select ENSP00000377934.3:p.Ser1281Ile
NM_198525.2:c.3842G>T (KIF7) NP_940927.2:p.Ser1281Ile
ENST00000394412.7:c.3842G>T (KIF7) ENSP00000377934.3:p.Ser1281Ile
ENST00000558928.1:n.172G>T (KIF7)
ENST00000561095.1:c.741-821C>A (TICRR)
ENST00000677187.1:n.1516G>T (KIF7)
ENST00000696512.1:c.3965G>T (KIF7) ENSP00000512678.1:p.Ser1322Ile
XM_005254902.2:c.3842G>T (KIF7) XP_005254959.1:p.Ser1281Ile
XM_011521531.1:c.3965G>T (KIF7) XP_011519833.1:p.Ser1322Ile
XM_011521531.2:c.3965G>T (KIF7) XP_011519833.1:p.Ser1322Ile
XM_011521532.1:c.3962G>T (KIF7) XP_011519834.1:p.Ser1321Ile
XM_011521533.1:c.3962G>T (KIF7) XP_011519835.1:p.Ser1321Ile
XM_011521534.1:c.3965G>T (KIF7) XP_011519836.1:p.Ser1322Ile
XM_011521535.1:c.3965G>T (KIF7) XP_011519837.1:p.Ser1322Ile
XM_011521536.1:c.3965G>T (KIF7) XP_011519838.1:p.Ser1322Ile