Canonical Allele Identifier: CA1315939291
Community Standard Title: NM_014362.4(HIBCH):c.941T= (p.Leu314=)
Gene: HIBCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190213026A= , CM000664.2:g.190213026A= GRCh38
NC_000002.11:g.191077752A= , CM000664.1:g.191077752A= GRCh37
NC_000002.10:g.190785997A= NCBI36
NG_017062.1:g.112020T=

Transcript Alleles

HGVS Amino-acid Change
NM_014362.4:c.941T= MANE Select NP_055177.2:p.Leu314=
ENST00000359678.10:c.941T= MANE Select ENSP00000352706.5:p.Leu314=
NM_014362.3:c.941T= NP_055177.2:p.Leu314=
NM_198047.2:c.941T= NP_932164.1:p.Leu314=
NM_198047.3:c.941T= NP_932164.1:p.Leu314=
ENST00000359678.9:c.941T= ENSP00000352706.5:p.Leu314=
ENST00000392332.7:c.941T= ENSP00000376144.3:p.Leu314=
ENST00000409820.2:c.281T= ENSP00000387098.2:p.Leu94=
ENST00000410045.5:c.272T= ENSP00000386274.1:p.Leu91=
ENST00000416732.5:c.194T= ENSP00000399263.1:p.Leu65=
ENST00000486981.1:n.210T=
ENST00000489147.1:n.3084T=
ENST00000622246.4:c.923T= ENSP00000481055.1:p.Leu308=
XM_011510953.1:c.941T= XP_011509255.1:p.Leu314=
XM_011510953.2:c.941T= XP_011509255.1:p.Leu314=
XM_011510954.1:c.443T= XP_011509256.1:p.Leu148=
XR_922903.1:n.1185T=
XR_922903.2:n.1004T=