Canonical Allele Identifier: CA352129102
Gene: DLEC1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38039461T>C , CM000665.2:g.38039461T>C GRCh38
NC_000003.11:g.38080952T>C , CM000665.1:g.38080952T>C GRCh37
NC_000003.10:g.38055956T>C NCBI36
NG_023237.1:g.5257T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308059.11:c.236T>C MANE Select ENSP00000308597.6:p.Leu79Pro
ENST00000308059.10:c.236T>C ENSP00000308597.6:p.Leu79Pro
ENST00000346219.7:c.236T>C ENSP00000315914.5:p.Leu79Pro
ENST00000440294.6:n.257T>C
NM_007335.2:c.236T>C NP_031361.2:p.Leu79Pro
NM_007337.2:c.236T>C NP_031363.2:p.Leu79Pro
XM_005265630.2:c.236T>C XP_005265687.1:p.Leu79Pro
XM_006713437.2:c.236T>C XP_006713500.1:p.Leu79Pro
XM_006713438.2:c.236T>C XP_006713501.1:p.Leu79Pro
XM_006713439.2:c.236T>C XP_006713502.1:p.Leu79Pro
XM_006713440.2:c.236T>C XP_006713503.1:p.Leu79Pro
XM_011534317.1:c.236T>C XP_011532619.1:p.Leu79Pro
XM_011534318.1:c.236T>C XP_011532620.1:p.Leu79Pro
XR_427301.2:n.857T>C
XR_427302.2:n.857T>C
XR_940527.1:n.857T>C
NM_001321153.1:c.236T>C NP_001308082.1:p.Leu79Pro
NM_007335.3:c.236T>C NP_031361.2:p.Leu79Pro
NM_007337.3:c.236T>C NP_031363.2:p.Leu79Pro
XM_006713438.3:c.236T>C XP_006713501.1:p.Leu79Pro
XM_006713439.3:c.236T>C XP_006713502.1:p.Leu79Pro
XM_006713440.3:c.236T>C XP_006713503.1:p.Leu79Pro
XM_011534317.2:c.236T>C XP_011532619.1:p.Leu79Pro
XM_011534318.2:c.236T>C XP_011532620.1:p.Leu79Pro
XR_427301.3:n.866T>C
XR_427302.3:n.867T>C
XR_940527.2:n.867T>C
NM_001321153.2:c.236T>C NP_001308082.1:p.Leu79Pro
NM_007335.4:c.236T>C MANE Select NP_031361.2:p.Leu79Pro
NM_007337.4:c.236T>C NP_031363.2:p.Leu79Pro