Canonical Allele Identifier: CA2569911937
Gene: UNC5C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537374A>T , CM000666.2:g.95537374A>T GRCh38
NC_000004.11:g.96458525A>T , CM000666.1:g.96458525A>T GRCh37
NC_000004.10:g.96677548A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11360T>A MANE Select ENSP00000406022.1:n.124+11360T>A
ENST00000453304.5:c.124+11360T>A ENSP00000406022.1:n.124+11360T>A
ENST00000504962.1:c.124+11360T>A ENSP00000425117.1:n.124+11360T>A
ENST00000506749.5:c.124+11360T>A ENSP00000426153.1:n.124+11360T>A
ENST00000513796.5:c.124+11360T>A ENSP00000426924.1:n.124+11360T>A
NM_003728.3:c.124+11360T>A NP_003719.3:n.124+11360T>A
XM_005263321.2:c.124+11360T>A XP_005263378.1:n.124+11360T>A
XM_005263321.3:c.124+11360T>A XP_005263378.1:n.124+11360T>A
NM_003728.4:c.124+11360T>A MANE Select NP_003719.3:n.124+11360T>A
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