Canonical Allele Identifier: CA565099704
Gene: TXNDC5 HGNC NCBI
BLOC1S5-TXNDC5 HGNC NCBI

Linked Data

dbSNP Id: rs1297484627
gnomAD v2: 6-7885214-C-T
gnomAD v3: 6-7884981-C-T
gnomAD v4: 6-7884981-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7884981C>T , CM000668.2:g.7884981C>T GRCh38
NC_000006.11:g.7885214C>T , CM000668.1:g.7885214C>T GRCh37
NC_000006.10:g.7830213C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379757.9:c.1047-493G>A (TXNDC5) MANE Select ENSP00000369081.4:n.1047-493G>A
ENST00000379757.8:c.1047-493G>A (TXNDC5) ENSP00000369081.4:n.1047-493G>A
ENST00000439343.2:c.1156-493G>A (BLOC1S5-TXNDC5) ENSP00000454697.1:n.1156-493G>A
ENST00000460138.5:n.825-493G>A (TXNDC5)
ENST00000473453.2:c.723-493G>A (TXNDC5) ENSP00000420784.1:n.723-493G>A
ENST00000475802.1:n.341-493G>A (TXNDC5)
NM_001145549.2:c.723-493G>A (TXNDC5) NP_001139021.1:n.723-493G>A
NM_030810.3:c.1047-493G>A (TXNDC5) NP_110437.2:n.1047-493G>A
NR_037616.1:n.1206-493G>A (BLOC1S5-TXNDC5)
NM_001145549.3:c.723-493G>A (TXNDC5) NP_001139021.1:n.723-493G>A
NM_030810.4:c.1047-493G>A (TXNDC5) NP_110437.2:n.1047-493G>A
NM_030810.5:c.1047-493G>A (TXNDC5) MANE Select NP_110437.2:n.1047-493G>A
NM_001145549.4:c.723-493G>A (TXNDC5) NP_001139021.1:n.723-493G>A