Canonical Allele Identifier: CA391381109

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386630A>C (hg19) ; chr15:g.28141484A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141484A>C , CM000677.2:g.28141484A>C	GRCh38
NC_000015.9:g.28386630A>C , CM000677.1:g.28386630A>C	GRCh37
NC_000015.8:g.26060225A>C	NCBI36
NG_016355.1:g.185666T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.11963T>G MANE Select	ENSP00000261609.8:p.Val3988Gly
ENST00000650509.1:c.3674T>G	ENSP00000496936.1:p.Val1225Gly
ENST00000261609.11:c.11963T>G	ENSP00000261609.7:p.Val3988Gly
NM_004667.5:c.11963T>G	NP_004658.3:p.Val3988Gly
XM_005268276.3:c.11849T>G	XP_005268333.1:p.Val3950Gly
XM_005268277.3:c.11849T>G	XP_005268334.1:p.Val3950Gly
XM_006720726.2:c.11948T>G	XP_006720789.1:p.Val3983Gly
XM_006720727.2:c.11705T>G	XP_006720790.1:p.Val3902Gly
XM_011522131.1:c.11480T>G	XP_011520433.1:p.Val3827Gly
XM_011522132.1:c.9479T>G	XP_011520434.1:p.Val3160Gly
XM_011522133.1:c.8708T>G	XP_011520435.1:p.Val2903Gly
XM_011522134.1:c.6080T>G	XP_011520436.1:p.Val2027Gly
XM_005268276.5:c.11849T>G	XP_005268333.1:p.Val3950Gly
XM_006720726.3:c.11948T>G	XP_006720789.1:p.Val3983Gly
XM_006720727.3:c.11705T>G	XP_006720790.1:p.Val3902Gly
XM_017022695.1:c.11849T>G	XP_016878184.1:p.Val3950Gly
XM_017022696.1:c.11849T>G	XP_016878185.1:p.Val3950Gly
XM_017022697.1:c.5129T>G	XP_016878186.1:p.Val1710Gly
XM_017022698.1:c.5129T>G	XP_016878187.1:p.Val1710Gly
NM_004667.6:c.11963T>G MANE Select	NP_004658.3:p.Val3988Gly