Canonical Allele Identifier: CA14214297
Gene: ABCC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16047966T>C , CM000678.2:g.16047966T>C GRCh38
NC_000016.9:g.16141823T>C , CM000678.1:g.16141823T>C GRCh37
NC_000016.8:g.16049324T>C NCBI36
NG_028268.1:g.103390T>C
NG_028268.2:g.103390T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.1219-176T>C ENSP00000382340.4:n.1219-176T>C
ENST00000399410.8:c.1219-176T>C MANE Select ENSP00000382342.3:n.1219-176T>C
ENST00000572882.3:c.1219-176T>C ENSP00000461615.2:n.1219-176T>C
ENST00000574224.2:n.1294-176T>C
ENST00000677164.1:c.1093-176T>C ENSP00000502873.1:n.1093-176T>C
ENST00000678422.1:c.1219-176T>C ENSP00000503954.1:n.1219-176T>C
ENST00000679043.1:n.1171-176T>C
ENST00000399408.6:c.241-176T>C ENSP00000382340.3:n.241-176T>C
ENST00000399410.7:c.1219-176T>C ENSP00000382342.3:n.1219-176T>C
ENST00000572882.2:c.914-176T>C
ENST00000574224.1:n.819-176T>C
NM_004996.3:c.1219-176T>C NP_004987.2:n.1219-176T>C
XM_011522497.1:c.1195-176T>C XP_011520799.1:n.1195-176T>C
XM_011522498.1:c.1273-176T>C XP_011520800.1:n.1273-176T>C
XM_011522498.2:c.1273-176T>C XP_011520800.1:n.1273-176T>C
XM_017023237.1:c.1273-176T>C XP_016878726.1:n.1273-176T>C
XM_017023238.1:c.1147-176T>C XP_016878727.1:n.1147-176T>C
XM_017023239.1:c.1135-176T>C XP_016878728.1:n.1135-176T>C
XM_017023240.1:c.1273-176T>C XP_016878729.1:n.1273-176T>C
XM_017023241.1:c.1009-176T>C XP_016878730.1:n.1009-176T>C
XM_017023242.1:c.1273-176T>C XP_016878731.1:n.1273-176T>C
XM_017023243.2:c.1273-176T>C XP_016878732.1:n.1273-176T>C
NM_004996.4:c.1219-176T>C MANE Select NP_004987.2:n.1219-176T>C
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