Canonical Allele Identifier: CA5242214
Community Standard Title: NM_001174147.2(LMX1B):c.115C>T (p.Pro39Ser)
Gene: LMX1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.126614564C>T , CM000671.2:g.126614564C>T GRCh38
NC_000009.11:g.129376843C>T , CM000671.1:g.129376843C>T GRCh37
NC_000009.10:g.128416664C>T NCBI36
NG_017039.1:g.5122C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001174147.2:c.115C>T MANE Select NP_001167618.1:p.Pro39Ser
ENST00000373474.9:c.115C>T MANE Select ENSP00000362573.3:p.Pro39Ser
NM_001174146.1:c.115C>T NP_001167617.1:p.Pro39Ser
NM_001174146.2:c.115C>T NP_001167617.1:p.Pro39Ser
NM_001174147.1:c.115C>T NP_001167618.1:p.Pro39Ser
NM_002316.3:c.115C>T NP_002307.2:p.Pro39Ser
NM_002316.4:c.115C>T NP_002307.2:p.Pro39Ser
ENST00000355497.10:c.115C>T ENSP00000347684.5:p.Pro39Ser
ENST00000355497.9:c.115C>T ENSP00000347684.5:p.Pro39Ser
ENST00000373474.8:c.115C>T ENSP00000362573.3:p.Pro39Ser
ENST00000526117.5:c.115C>T ENSP00000436930.1:p.Pro39Ser
ENST00000526117.6:c.115C>T ENSP00000436930.1:p.Pro39Ser
ENST00000561065.1:c.46C>T ENSP00000453580.1:p.Pro16Ser