Canonical Allele Identifier: CA5940383

Gene: KIAA1549L

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.33646010A>G , CM000673.2:g.33646010A>G	GRCh38
NC_000011.9:g.33667556A>G , CM000673.1:g.33667556A>G	GRCh37
NC_000011.8:g.33624132A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012194.3:c.5734A>G MANE Select	NP_036326.3:p.Met1912Val
ENST00000658780.2:c.5734A>G MANE Select	ENSP00000499430.1:p.Met1912Val
NM_012194.2:c.4843A>G	NP_036326.2:p.Met1615Val
ENST00000321505.8:c.4843A>G	ENSP00000315295.4:p.Met1615Val
ENST00000321505.9:c.4843A>G	ENSP00000315295.4:p.Met1615Val
ENST00000526400.7:c.3544A>G	ENSP00000433481.3:p.Met1182Val
XM_005252847.2:c.4978A>G	XP_005252904.2:p.Met1660Val
XM_005252847.3:c.4978A>G	XP_005252904.2:p.Met1660Val
XM_005252848.2:c.4858A>G	XP_005252905.1:p.Met1620Val
XM_005252848.3:c.4858A>G	XP_005252905.1:p.Met1620Val
XM_011519970.1:c.3544A>G	XP_011518272.1:p.Met1182Val
XM_011519970.2:c.3544A>G	XP_011518272.1:p.Met1182Val
XM_017017484.2:c.4861A>G	XP_016872973.1:p.Met1621Val
XM_017017486.1:c.3541A>G	XP_016872975.1:p.Met1181Val