Canonical Allele Identifier: CA349894347
Community Standard Title: NM_014362.4(HIBCH):c.938A>C (p.Gln313Pro)
Gene: HIBCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190213029T>G , CM000664.2:g.190213029T>G GRCh38
NC_000002.11:g.191077755T>G , CM000664.1:g.191077755T>G GRCh37
NC_000002.10:g.190786000T>G NCBI36
NG_017062.1:g.112017A>C

Transcript Alleles

HGVS Amino-acid Change
NM_014362.4:c.938A>C MANE Select NP_055177.2:p.Gln313Pro
ENST00000359678.10:c.938A>C MANE Select ENSP00000352706.5:p.Gln313Pro
NM_014362.3:c.938A>C NP_055177.2:p.Gln313Pro
NM_198047.2:c.938A>C NP_932164.1:p.Gln313Pro
NM_198047.3:c.938A>C NP_932164.1:p.Gln313Pro
ENST00000359678.9:c.938A>C ENSP00000352706.5:p.Gln313Pro
ENST00000392332.7:c.938A>C ENSP00000376144.3:p.Gln313Pro
ENST00000409820.2:c.278A>C ENSP00000387098.2:p.Gln93Pro
ENST00000410045.5:c.269A>C ENSP00000386274.1:p.Gln90Pro
ENST00000416732.5:c.191A>C ENSP00000399263.1:p.Gln64Pro
ENST00000486981.1:n.207A>C
ENST00000489147.1:n.3081A>C
ENST00000622246.4:c.920A>C ENSP00000481055.1:p.Gln307Pro
XM_011510953.1:c.938A>C XP_011509255.1:p.Gln313Pro
XM_011510953.2:c.938A>C XP_011509255.1:p.Gln313Pro
XM_011510954.1:c.440A>C XP_011509256.1:p.Gln147Pro
XR_922903.1:n.1182A>C
XR_922903.2:n.1001A>C