Canonical Allele Identifier: CA1865983183
Gene: HSD17B3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96240885G= , CM000671.2:g.96240885G= GRCh38
NC_000009.11:g.99003167G= , CM000671.1:g.99003167G= GRCh37
NC_000009.10:g.98042988G= NCBI36
NG_008157.1:g.66268C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375262.4:c.672+3444C= ENSP00000364411.2:n.672+3444C=
ENST00000375263.8:c.695C= MANE Select ENSP00000364412.3:p.Ser232=
ENST00000463517.2:n.2237C=
ENST00000464104.6:n.1633C=
ENST00000467499.6:c.*394C= ENSP00000498077.1:n.*394C=
ENST00000484816.2:n.46C=
ENST00000494814.6:n.245C=
ENST00000643789.1:c.2987C=
ENST00000648146.1:c.695C= ENSP00000497238.1:p.Ser232=
ENST00000648332.1:c.372C= ENSP00000497562.1:n.372C=
ENST00000648799.1:c.587C= ENSP00000498039.1:p.Ser196=
ENST00000650005.1:c.624C= ENSP00000498121.1:n.624C=
ENST00000375262.3:c.672+3444C= ENSP00000364411.2:n.672+3444C=
ENST00000375263.7:c.695C= ENSP00000364412.3:p.Ser232=
ENST00000464104.5:n.548C=
ENST00000484816.1:n.45C=
ENST00000494814.5:n.254C=
NM_000197.1:c.695C= NP_000188.1:p.Ser232=
XM_005251970.3:c.335C= XP_005252027.1:p.Ser112=
XM_011518618.1:c.695C= XP_011516920.1:p.Ser232=
XM_011518619.1:c.695C= XP_011516921.1:p.Ser232=
XM_011518620.1:c.587C= XP_011516922.1:p.Ser196=
XM_011518621.1:c.*16C= XP_011516923.1:n.*16C=
NM_000197.2:c.695C= MANE Select NP_000188.1:p.Ser232=
XM_011518618.2:c.695C= XP_011516920.1:p.Ser232=
XM_011518619.2:c.695C= XP_011516921.1:p.Ser232=
XM_017014671.1:c.695C= XP_016870160.1:p.Ser232=
XM_017014672.1:c.695C= XP_016870161.1:p.Ser232=
XM_017014673.2:c.659C= XP_016870162.1:p.Ser220=
XM_017014674.1:c.587C= XP_016870163.1:p.Ser196=
XM_017014675.1:c.533C= XP_016870164.1:p.Ser178=
XM_017014677.1:c.335C= XP_016870166.1:p.Ser112=
XM_024447529.1:c.533C= XP_024303297.1:p.Ser178=
XR_002956778.1:n.3167C=