Canonical Allele Identifier: CA15592974

Gene: STX17

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99961410C>T , CM000671.2:g.99961410C>T	GRCh38
NC_000009.11:g.102723692C>T , CM000671.1:g.102723692C>T	GRCh37
NC_000009.10:g.101763513C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259400.11:c.582+1255C>T MANE Select	ENSP00000259400.6:n.582+1255C>T
ENST00000259400.10:c.582+1255C>T	ENSP00000259400.6:n.582+1255C>T
ENST00000524405.5:c.*40+1255C>T	ENSP00000436666.1:n.*40+1255C>T
ENST00000525640.5:c.582+1255C>T	ENSP00000435981.1:n.582+1255C>T
ENST00000525847.1:n.562+1255C>T
ENST00000529340.5:c.*448+1255C>T	ENSP00000434323.1:n.*448+1255C>T
ENST00000534052.1:c.582+1255C>T	ENSP00000433484.1:n.582+1255C>T
NM_017919.2:c.582+1255C>T	NP_060389.2:n.582+1255C>T
XM_011518820.1:c.582+1255C>T	XP_011517122.1:n.582+1255C>T
XM_011518821.1:c.582+1255C>T	XP_011517123.1:n.582+1255C>T
XM_011518822.1:c.582+1255C>T	XP_011517124.1:n.582+1255C>T
XM_011518823.1:c.315+1255C>T	XP_011517125.1:n.315+1255C>T
XR_929815.1:n.680+1255C>T
XM_011518820.3:c.582+1255C>T	XP_011517122.1:n.582+1255C>T
XM_011518821.3:c.582+1255C>T	XP_011517123.1:n.582+1255C>T
XM_011518823.3:c.315+1255C>T	XP_011517125.1:n.315+1255C>T
XM_017014875.2:c.315+1255C>T	XP_016870364.1:n.315+1255C>T
XM_024447593.1:c.315+1255C>T	XP_024303361.1:n.315+1255C>T
NM_017919.3:c.582+1255C>T MANE Select	NP_060389.2:n.582+1255C>T