Canonical Allele Identifier: CA391381964

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386949A>T (hg19) ; chr15:g.28141803A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141803A>T , CM000677.2:g.28141803A>T	GRCh38
NC_000015.9:g.28386949A>T , CM000677.1:g.28386949A>T	GRCh37
NC_000015.8:g.26060544A>T	NCBI36
NG_016355.1:g.185347T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11744T>A MANE Select	ENSP00000261609.8:p.Met3915Lys
ENST00000650509.1:c.3455T>A	ENSP00000496936.1:p.Met1152Lys
ENST00000261609.11:c.11744T>A	ENSP00000261609.7:p.Met3915Lys
ENST00000564519.1:n.259T>A
NM_004667.5:c.11744T>A	NP_004658.3:p.Met3915Lys
XM_005268276.3:c.11630T>A	XP_005268333.1:p.Met3877Lys
XM_005268277.3:c.11630T>A	XP_005268334.1:p.Met3877Lys
XM_006720726.2:c.11729T>A	XP_006720789.1:p.Met3910Lys
XM_006720727.2:c.11486T>A	XP_006720790.1:p.Met3829Lys
XM_011522131.1:c.11261T>A	XP_011520433.1:p.Met3754Lys
XM_011522132.1:c.9260T>A	XP_011520434.1:p.Met3087Lys
XM_011522133.1:c.8489T>A	XP_011520435.1:p.Met2830Lys
XM_011522134.1:c.5861T>A	XP_011520436.1:p.Met1954Lys
XM_005268276.5:c.11630T>A	XP_005268333.1:p.Met3877Lys
XM_006720726.3:c.11729T>A	XP_006720789.1:p.Met3910Lys
XM_006720727.3:c.11486T>A	XP_006720790.1:p.Met3829Lys
XM_017022695.1:c.11630T>A	XP_016878184.1:p.Met3877Lys
XM_017022696.1:c.11630T>A	XP_016878185.1:p.Met3877Lys
XM_017022697.1:c.4910T>A	XP_016878186.1:p.Met1637Lys
XM_017022698.1:c.4910T>A	XP_016878187.1:p.Met1637Lys
NM_004667.6:c.11744T>A MANE Select	NP_004658.3:p.Met3915Lys