Canonical Allele Identifier: CA358080519

Gene: BLTP1

Linked Data

• MyVariant Identifiers: chr4:g.123147974G>T (hg19) ; chr4:g.122226819G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122226819G>T , CM000666.2:g.122226819G>T	GRCh38
NC_000004.11:g.123147974G>T , CM000666.1:g.123147974G>T	GRCh37
NC_000004.10:g.123367424G>T	NCBI36
NG_015813.1:g.61217G>T
NG_015813.2:g.61217G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388738.8:c.2906G>T	ENSP00000373390.4:p.Arg969Leu
ENST00000424425.6:c.1005G>T
ENST00000684987.1:n.3229G>T
ENST00000686075.1:n.3229G>T
ENST00000687476.1:n.3047G>T
ENST00000689316.1:n.1371G>T
ENST00000690536.1:n.3229G>T
ENST00000693334.1:n.3229G>T
ENST00000693420.1:c.2906G>T	ENSP00000509435.1:p.Arg969Leu
ENST00000679879.1:c.2906G>T MANE Select	ENSP00000505357.1:p.Arg969Leu
ENST00000264501.8:c.2906G>T	ENSP00000264501.4:p.Arg969Leu
ENST00000388738.7:c.2906G>T	ENSP00000373390.3:p.Arg969Leu
ENST00000424425.5:c.2400G>T
ENST00000449251.1:c.417+2142G>T	ENSP00000413018.1:n.417+2142G>T
ENST00000482114.1:n.3168G>T
ENST00000495260.5:n.1604G>T
NM_015312.3:c.2906G>T	NP_056127.2:p.Arg969Leu
XM_005263282.1:c.2906G>T	XP_005263339.1:p.Arg969Leu
XM_005263287.1:c.2906G>T	XP_005263344.1:p.Arg969Leu
XM_006714343.1:c.2906G>T	XP_006714406.1:p.Arg969Leu
XM_006714344.1:c.2903G>T	XP_006714407.1:p.Arg968Leu
XM_011532319.1:c.2906G>T	XP_011530621.1:p.Arg969Leu
XM_011532320.1:c.2906G>T	XP_011530622.1:p.Arg969Leu
XM_011532321.1:c.2906G>T	XP_011530623.1:p.Arg969Leu
XM_011532322.1:c.2903G>T	XP_011530624.1:p.Arg968Leu
XM_011532323.1:c.2906G>T	XP_011530625.1:p.Arg969Leu
XM_011532324.1:c.2906G>T	XP_011530626.1:p.Arg969Leu
XM_011532325.1:c.2906G>T	XP_011530627.1:p.Arg969Leu
XM_011532326.1:c.2793+2142G>T	XP_011530628.1:n.2793+2142G>T
XM_011532327.1:c.2756G>T	XP_011530629.1:p.Arg919Leu
XM_011532328.1:c.2906G>T	XP_011530630.1:p.Arg969Leu
XM_011532329.1:c.2906G>T	XP_011530631.1:p.Arg969Leu
XM_011532330.1:c.1157G>T	XP_011530632.1:p.Arg386Leu
XM_011532331.1:c.2906G>T	XP_011530633.1:p.Arg969Leu
XR_938781.1:n.3279G>T
XR_938782.1:n.3279G>T
XR_938783.1:n.3279G>T
XM_011532320.3:c.2906G>T	XP_011530622.1:p.Arg969Leu
XM_011532321.2:c.2906G>T	XP_011530623.1:p.Arg969Leu
XM_017008695.1:c.2906G>T	XP_016864184.1:p.Arg969Leu
XM_017008696.1:c.2906G>T	XP_016864185.1:p.Arg969Leu
XM_017008697.1:c.2906G>T	XP_016864186.1:p.Arg969Leu
XM_017008698.1:c.137G>T	XP_016864187.1:p.Arg46Leu
XM_017008699.1:c.2906G>T	XP_016864188.1:p.Arg969Leu
XM_024454243.1:c.1058G>T	XP_024310011.1:p.Arg353Leu
XR_001741335.2:n.3279G>T
XR_001741336.1:n.3279G>T
XR_001741337.1:n.3279G>T
NM_001384125.1:c.2906G>T MANE Select	NP_001371054.1:p.Arg969Leu
NM_015312.4:c.2906G>T	NP_056127.2:p.Arg969Leu