Canonical Allele Identifier: CA8612260

Gene: HEXIM2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45169117G>C , CM000679.2:g.45169117G>C	GRCh38
NC_000017.10:g.43246484G>C , CM000679.1:g.43246484G>C	GRCh37
NC_000017.9:g.40602267G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585340.2:c.169G>C	ENSP00000468251.2:p.Asp57His
ENST00000586681.6:c.169G>C	ENSP00000465086.2:p.Asp57His
ENST00000589230.6:c.169G>C MANE Select	ENSP00000466200.2:p.Asp57His
ENST00000591070.6:c.169G>C	ENSP00000464807.2:p.Asp57His
ENST00000593138.6:c.169G>C	ENSP00000468773.2:p.Asp57His
ENST00000307275.7:c.169G>C	ENSP00000302276.2:p.Asp57His
ENST00000585340.1:c.235G>C	ENSP00000468251.1:p.Asp79His
ENST00000586681.5:c.169G>C	ENSP00000465086.1:p.Asp57His
ENST00000589230.5:c.169G>C	ENSP00000466200.1:p.Asp57His
ENST00000591070.5:c.169G>C	ENSP00000464807.1:p.Asp57His
ENST00000591576.5:c.169G>C	ENSP00000465727.1:p.Asp57His
ENST00000592695.1:c.169G>C	ENSP00000467517.1:p.Asp57His
ENST00000593138.5:c.169G>C	ENSP00000468773.1:p.Asp57His
NM_001303436.1:c.235G>C	NP_001290365.1:p.Asp79His
NM_001303437.1:c.169G>C	NP_001290366.1:p.Asp57His
NM_001303438.1:c.169G>C	NP_001290367.1:p.Asp57His
NM_001303439.1:c.169G>C	NP_001290368.1:p.Asp57His
NM_001303440.1:c.169G>C	NP_001290369.1:p.Asp57His
NM_001303441.1:c.169G>C	NP_001290370.1:p.Asp57His
NM_001303442.1:c.169G>C	NP_001290371.1:p.Asp57His
NM_001303443.1:c.169G>C	NP_001290372.1:p.Asp57His
NM_001303444.1:c.169G>C	NP_001290373.1:p.Asp57His
NM_144608.2:c.169G>C	NP_653209.1:p.Asp57His
XM_006721687.2:c.238G>C	XP_006721750.1:p.Asp80His
XM_011524302.1:c.169G>C	XP_011522604.1:p.Asp57His
XM_011524303.1:c.169G>C	XP_011522605.1:p.Asp57His
XM_011524304.1:c.169G>C	XP_011522606.1:p.Asp57His
XM_011524305.1:c.169G>C	XP_011522607.1:p.Asp57His
XM_011524306.1:c.169G>C	XP_011522608.1:p.Asp57His
XM_011524307.1:c.169G>C	XP_011522609.1:p.Asp57His
XM_011524308.1:c.169G>C	XP_011522610.1:p.Asp57His
XR_934782.1:n.1736C>G
NR_135646.1:n.1736C>G
XM_006721687.4:c.238G>C	XP_006721750.1:p.Asp80His
XM_011524306.2:c.169G>C	XP_011522608.1:p.Asp57His
XM_011524307.3:c.169G>C	XP_011522609.3:p.Asp57His
XM_011524308.3:c.169G>C	XP_011522610.3:p.Asp57His
XM_017024167.2:c.169G>C	XP_016879656.1:p.Asp57His
XM_017024170.2:c.169G>C	XP_016879659.1:p.Asp57His
XM_024450566.1:c.169G>C	XP_024306334.1:p.Asp57His
XM_024450567.1:c.169G>C	XP_024306335.1:p.Asp57His
XM_024450568.1:c.169G>C	XP_024306336.1:p.Asp57His
NM_001303440.2:c.169G>C	NP_001290369.1:p.Asp57His
NM_001303441.2:c.169G>C MANE Select	NP_001290370.1:p.Asp57His
NM_001303442.2:c.169G>C	NP_001290371.1:p.Asp57His
NM_001303443.2:c.169G>C	NP_001290372.1:p.Asp57His
NM_001303444.2:c.169G>C	NP_001290373.1:p.Asp57His