Canonical Allele Identifier: CA3237111

Gene: NIPBL

Linked Data

• dbSNP Id: rs762029831
• ExAC: 5:37051927 T / C
• gnomAD v2: 5-37051927-T-C
• gnomAD v4: 5-37051825-T-C
• MyVariant Identifiers: chr5:g.37051927T>C (hg19) ; chr5:g.37051825T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051825T>C , CM000667.2:g.37051825T>C	GRCh38
NC_000005.9:g.37051927T>C , CM000667.1:g.37051927T>C	GRCh37
NC_000005.8:g.37087684T>C	NCBI36
NG_006987.1:g.179943T>C
NG_006987.2:g.179943T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7001T>C MANE Select	ENSP00000282516.8:p.Met2334Thr
ENST00000652901.1:c.7001T>C	ENSP00000499536.1:p.Met2334Thr
ENST00000282516.12:c.7001T>C	ENSP00000282516.8:p.Met2334Thr
ENST00000448238.2:c.7001T>C	ENSP00000406266.2:p.Met2334Thr
ENST00000514335.1:n.883T>C
ENST00000621733.1:c.1-12753T>C	ENSP00000480694.1:n.1-12753T>C
NM_015384.4:c.7001T>C	NP_056199.2:p.Met2334Thr
NM_133433.3:c.7001T>C	NP_597677.2:p.Met2334Thr
XM_005248280.2:c.7001T>C	XP_005248337.1:p.Met2334Thr
XM_005248282.3:c.6257T>C	XP_005248339.2:p.Met2086Thr
XM_006714467.2:c.7001T>C	XP_006714530.1:p.Met2334Thr
XM_006714468.1:c.6803T>C	XP_006714531.1:p.Met2268Thr
XM_011514014.1:c.6620T>C	XP_011512316.1:p.Met2207Thr
XM_011514015.1:c.7001T>C	XP_011512317.1:p.Met2334Thr
XM_005248280.3:c.7001T>C	XP_005248337.1:p.Met2334Thr
XM_005248282.5:c.6341T>C	XP_005248339.3:p.Met2114Thr
XM_006714468.2:c.6803T>C	XP_006714531.1:p.Met2268Thr
XM_017009329.1:c.7001T>C	XP_016864818.1:p.Met2334Thr
XM_017009330.2:c.5384T>C	XP_016864819.1:p.Met1795Thr
XM_017009331.1:c.5375T>C	XP_016864820.1:p.Met1792Thr
NM_133433.4:c.7001T>C MANE Select	NP_597677.2:p.Met2334Thr
NM_015384.5:c.7001T>C	NP_056199.2:p.Met2334Thr