Canonical Allele Identifier: CA391381923

Gene: HERC2

Linked Data

• dbSNP Id: rs569374388
• gnomAD v2: 15-28386931-C-G
• gnomAD v3: 15-28141785-C-G
• gnomAD v4: 15-28141785-C-G
• MyVariant Identifiers: chr15:g.28386931C>G (hg19) ; chr15:g.28141785C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141785C>G , CM000677.2:g.28141785C>G	GRCh38
NC_000015.9:g.28386931C>G , CM000677.1:g.28386931C>G	GRCh37
NC_000015.8:g.26060526C>G	NCBI36
NG_016355.1:g.185365G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11762G>C MANE Select	ENSP00000261609.8:p.Ser3921Thr
ENST00000650509.1:c.3473G>C	ENSP00000496936.1:p.Ser1158Thr
ENST00000261609.11:c.11762G>C	ENSP00000261609.7:p.Ser3921Thr
ENST00000564519.1:n.277G>C
NM_004667.5:c.11762G>C	NP_004658.3:p.Ser3921Thr
XM_005268276.3:c.11648G>C	XP_005268333.1:p.Ser3883Thr
XM_005268277.3:c.11648G>C	XP_005268334.1:p.Ser3883Thr
XM_006720726.2:c.11747G>C	XP_006720789.1:p.Ser3916Thr
XM_006720727.2:c.11504G>C	XP_006720790.1:p.Ser3835Thr
XM_011522131.1:c.11279G>C	XP_011520433.1:p.Ser3760Thr
XM_011522132.1:c.9278G>C	XP_011520434.1:p.Ser3093Thr
XM_011522133.1:c.8507G>C	XP_011520435.1:p.Ser2836Thr
XM_011522134.1:c.5879G>C	XP_011520436.1:p.Ser1960Thr
XM_005268276.5:c.11648G>C	XP_005268333.1:p.Ser3883Thr
XM_006720726.3:c.11747G>C	XP_006720789.1:p.Ser3916Thr
XM_006720727.3:c.11504G>C	XP_006720790.1:p.Ser3835Thr
XM_017022695.1:c.11648G>C	XP_016878184.1:p.Ser3883Thr
XM_017022696.1:c.11648G>C	XP_016878185.1:p.Ser3883Thr
XM_017022697.1:c.4928G>C	XP_016878186.1:p.Ser1643Thr
XM_017022698.1:c.4928G>C	XP_016878187.1:p.Ser1643Thr
NM_004667.6:c.11762G>C MANE Select	NP_004658.3:p.Ser3921Thr