Canonical Allele Identifier: CA1621058581

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35797291T= , CM000668.2:g.35797291T= GRCh38
NC_000006.11:g.35765068T= , CM000668.1:g.35765068T= GRCh37
NC_000006.10:g.35873046T= NCBI36
NG_012184.3:g.5086T=

Transcript Alleles

HGVS Amino-acid Change
NM_001832.4:c.-3A= (CLPS) MANE Select NP_001823.1:n.-3A=
ENST00000259938.7:c.-3A= (CLPS) MANE Select ENSP00000259938.2:n.-3A=
NM_001252597.1:c.-143A= (CLPS) NP_001239526.1:n.-143A=
NM_001252597.2:c.-143A= (CLPS) NP_001239526.1:n.-143A=
NM_001252598.1:c.-3A= (CLPS) NP_001239527.1:n.-3A=
NM_001252598.2:c.-3A= (CLPS) NP_001239527.1:n.-3A=
NM_001832.3:c.-3A= (CLPS) NP_001823.1:n.-3A=
ENST00000259938.6:c.-3A= (CLPS) ENSP00000259938.2:n.-3A=
ENST00000616014.3:c.-3A= (CLPS) ENSP00000483589.1:n.-3A=
ENST00000651132.1:c.-323+2T= (LHFPL5) ENSP00000498322.1:n.-323+2T=