Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076627A= , CM000676.2:g.65076627A=	GRCh38
NC_000014.8:g.65543345A= , CM000676.1:g.65543345A=	GRCh37
NC_000014.7:g.64613098A=	NCBI36
NG_029830.1:g.30883T= , LRG_530:g.30883T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.113T=	ENSP00000452206.2:p.Leu38=
ENST00000556979.6:c.*785T=	ENSP00000452378.1:n.*785T=
ENST00000358664.9:c.332T= MANE Select	ENSP00000351490.4:p.Leu111=
ENST00000651648.1:c.145-6258T=	ENSP00000498863.1:n.145-6258T=
ENST00000284165.10:c.*1176T=	ENSP00000284165.6:n.*1176T=
ENST00000341653.6:c.171+17081T=	ENSP00000342482.2:n.171+17081T=
ENST00000358402.8:c.305T=	ENSP00000351175.4:p.Leu102=
ENST00000358664.8:c.332T=	ENSP00000351490.4:p.Leu111=
ENST00000394606.6:c.*105T=	ENSP00000378104.2:n.*105T=
ENST00000553928.5:c.*121T=	ENSP00000451907.1:n.*121T=
ENST00000555419.5:c.224T=	ENSP00000452405.1:p.Leu75=
ENST00000555932.5:c.73T=	ENSP00000450763.1:p.Cys25=
ENST00000556892.5:c.113T=	ENSP00000452206.1:p.Leu38=
ENST00000557277.5:c.143T=	ENSP00000450955.1:p.Leu48=
ENST00000618858.4:c.*121T=	ENSP00000480127.1:n.*121T=
NM_001271069.1:c.144+17081T=	NP_001257998.1:n.144+17081T=
NM_002382.4:c.332T=	NP_002373.3:p.Leu111=
NM_145112.2:c.305T=	NP_660087.1:p.Leu102=
NM_145113.2:c.*121T=	NP_660088.1:n.*121T=
NM_197957.3:c.171+17081T=	NP_932061.1:n.171+17081T=
NR_073137.1:n.456T=
XR_429315.2:n.619T=
XR_943450.1:n.700T=
XR_943451.1:n.716T=
XR_943452.1:n.662T=
NM_001320415.1:c.143T=	NP_001307344.1:p.Leu48=
XM_017021312.2:c.143T=	XP_016876801.1:p.Leu48=
XM_017021313.1:c.143T=	XP_016876802.1:p.Leu48=
XR_001750326.2:n.677T=
XR_001750327.2:n.596T=
XR_002957553.1:n.1110T=
XR_943450.3:n.700T=
XR_943451.3:n.716T=
XR_943452.3:n.661T=
NM_001320415.2:c.143T=	NP_001307344.1:p.Leu48=
NM_002382.5:c.332T= MANE Select	NP_002373.3:p.Leu111=
NM_145112.3:c.305T=	NP_660087.1:p.Leu102=
NM_145113.3:c.*121T=	NP_660088.1:n.*121T=
NM_001271069.2:c.144+17081T=	NP_001257998.1:n.144+17081T=
NM_197957.4:c.171+17081T=	NP_932061.1:n.171+17081T=