Canonical Allele Identifier: CA8164252
Community Standard Title: NM_006885.4(ZFHX3):c.2915C>T (p.Ser972Leu)
Gene: ZFHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72950770G>A , CM000678.2:g.72950770G>A GRCh38
NC_000016.9:g.72984669G>A , CM000678.1:g.72984669G>A GRCh37
NC_000016.8:g.71542170G>A NCBI36
NG_013211.1:g.112866C>T
NG_013211.2:g.946162C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006885.4:c.2915C>T MANE Select NP_008816.3:p.Ser972Leu
ENST00000268489.10:c.2915C>T MANE Select ENSP00000268489.5:p.Ser972Leu
NM_001164766.1:c.173C>T NP_001158238.1:p.Ser58Leu
NM_001164766.2:c.173C>T NP_001158238.1:p.Ser58Leu
NM_001386735.1:c.2915C>T NP_001373664.1:p.Ser972Leu
NM_006885.3:c.2915C>T NP_008816.3:p.Ser972Leu
ENST00000268489.9:c.2915C>T ENSP00000268489.5:p.Ser972Leu
ENST00000397992.5:c.173C>T ENSP00000438926.3:p.Ser58Leu
ENST00000641206.2:c.2915C>T ENSP00000493252.1:p.Ser972Leu
XM_005255957.2:c.2915C>T XP_005256014.1:p.Ser972Leu
XM_005255957.4:c.2915C>T XP_005256014.1:p.Ser972Leu
XM_017023251.2:c.266C>T XP_016878740.1:p.Ser89Leu
XM_024450291.1:c.266C>T XP_024306059.1:p.Ser89Leu