Canonical Allele Identifier: CA391382005

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386966C>G (hg19) ; chr15:g.28141820C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141820C>G , CM000677.2:g.28141820C>G	GRCh38
NC_000015.9:g.28386966C>G , CM000677.1:g.28386966C>G	GRCh37
NC_000015.8:g.26060561C>G	NCBI36
NG_016355.1:g.185330G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11727G>C MANE Select	ENSP00000261609.8:p.Met3909Ile
ENST00000650509.1:c.3438G>C	ENSP00000496936.1:p.Met1146Ile
ENST00000261609.11:c.11727G>C	ENSP00000261609.7:p.Met3909Ile
ENST00000564519.1:n.242G>C
NM_004667.5:c.11727G>C	NP_004658.3:p.Met3909Ile
XM_005268276.3:c.11613G>C	XP_005268333.1:p.Met3871Ile
XM_005268277.3:c.11613G>C	XP_005268334.1:p.Met3871Ile
XM_006720726.2:c.11712G>C	XP_006720789.1:p.Met3904Ile
XM_006720727.2:c.11469G>C	XP_006720790.1:p.Met3823Ile
XM_011522131.1:c.11244G>C	XP_011520433.1:p.Met3748Ile
XM_011522132.1:c.9243G>C	XP_011520434.1:p.Met3081Ile
XM_011522133.1:c.8472G>C	XP_011520435.1:p.Met2824Ile
XM_011522134.1:c.5844G>C	XP_011520436.1:p.Met1948Ile
XM_005268276.5:c.11613G>C	XP_005268333.1:p.Met3871Ile
XM_006720726.3:c.11712G>C	XP_006720789.1:p.Met3904Ile
XM_006720727.3:c.11469G>C	XP_006720790.1:p.Met3823Ile
XM_017022695.1:c.11613G>C	XP_016878184.1:p.Met3871Ile
XM_017022696.1:c.11613G>C	XP_016878185.1:p.Met3871Ile
XM_017022697.1:c.4893G>C	XP_016878186.1:p.Met1631Ile
XM_017022698.1:c.4893G>C	XP_016878187.1:p.Met1631Ile
NM_004667.6:c.11727G>C MANE Select	NP_004658.3:p.Met3909Ile