Canonical Allele Identifier: CA1962830748
Gene: KIAA1549L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.33566628G= , CM000673.2:g.33566628G= GRCh38
NC_000011.9:g.33588174G= , CM000673.1:g.33588174G= GRCh37
NC_000011.8:g.33544750G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000526400.7:c.1889-1448G= ENSP00000433481.3:n.1889-1448G=
ENST00000265654.6:c.3330-1448G=
ENST00000321505.9:c.3188-1448G= ENSP00000315295.4:n.3188-1448G=
ENST00000526400.6:c.1889-1448G= ENSP00000433481.2:n.1889-1448G=
ENST00000658780.2:c.4079-1448G= MANE Select ENSP00000499430.1:n.4079-1448G=
ENST00000265654.5:c.3206-1448G= ENSP00000265654.5:n.3206-1448G=
ENST00000321505.8:c.3188-1448G= ENSP00000315295.4:n.3188-1448G=
ENST00000526400.5:c.1381-1448G=
NM_012194.2:c.3188-1448G= NP_036326.2:n.3188-1448G=
XM_005252847.2:c.3323-1448G= XP_005252904.2:n.3323-1448G=
XM_005252848.2:c.3206-1448G= XP_005252905.1:n.3206-1448G=
XM_011519969.1:c.3206-1448G= XP_011518271.1:n.3206-1448G=
XM_011519970.1:c.1889-1448G= XP_011518272.1:n.1889-1448G=
XM_005252847.3:c.3323-1448G= XP_005252904.2:n.3323-1448G=
XM_005252848.3:c.3206-1448G= XP_005252905.1:n.3206-1448G=
XM_011519969.2:c.3206-1448G= XP_011518271.1:n.3206-1448G=
XM_011519970.2:c.1889-1448G= XP_011518272.1:n.1889-1448G=
XM_017017484.2:c.3206-1448G= XP_016872973.1:n.3206-1448G=
XM_017017486.1:c.1889-1448G= XP_016872975.1:n.1889-1448G=
NM_012194.3:c.4079-1448G= MANE Select NP_036326.3:n.4079-1448G=