Canonical Allele Identifier: CA2817728791

Gene: SYNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32656984A>G , CM000683.2:g.32656984A>G	GRCh38
NC_000021.8:g.34029294A>G , CM000683.1:g.34029294A>G	GRCh37
NC_000021.7:g.32951165A>G	NCBI36
NG_030017.1:g.76058T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382499.7:c.2696+19T>C	ENSP00000371939.2:n.2696+19T>C
ENST00000433931.7:c.2696+19T>C	ENSP00000409667.2:n.2696+19T>C
ENST00000630077.3:c.2564+19T>C	ENSP00000487560.1:n.2564+19T>C
ENST00000674204.1:c.2579+19T>C	ENSP00000501504.1:n.2579+19T>C
ENST00000674308.1:c.2579+19T>C	ENSP00000501426.1:n.2579+19T>C
ENST00000674351.1:c.2579+19T>C MANE Select	ENSP00000501530.1:n.2579+19T>C
ENST00000357345.7:c.2579+19T>C	ENSP00000349903.3:n.2579+19T>C
ENST00000382491.7:c.2564+19T>C	ENSP00000371931.4:n.2564+19T>C
ENST00000382499.6:c.2696+19T>C	ENSP00000371939.2:n.2696+19T>C
ENST00000433931.6:c.2696+19T>C	ENSP00000409667.2:n.2696+19T>C
ENST00000464778.1:n.366+19T>C
ENST00000630077.2:c.2564+19T>C	ENSP00000487560.1:n.2564+19T>C
NM_001160302.1:c.2579+19T>C	NP_001153774.1:n.2579+19T>C
NM_001160306.1:c.2564+19T>C	NP_001153778.1:n.2564+19T>C
NM_003895.3:c.2696+19T>C	NP_003886.3:n.2696+19T>C
NM_203446.2:c.2696+19T>C	NP_982271.2:n.2696+19T>C
XM_017028494.1:c.2579+19T>C	XP_016883983.1:n.2579+19T>C
XM_017028495.2:c.2681+19T>C	XP_016883984.1:n.2681+19T>C
XM_017028496.1:c.2579+19T>C	XP_016883985.1:n.2579+19T>C
XM_017028497.2:c.2696+19T>C	XP_016883986.1:n.2696+19T>C
XM_017028498.1:c.2579+19T>C	XP_016883987.1:n.2579+19T>C
XM_017028499.2:c.2681+19T>C	XP_016883988.1:n.2681+19T>C
XM_017028500.1:c.2579+19T>C	XP_016883989.1:n.2579+19T>C
XM_017028501.1:c.2579+19T>C	XP_016883990.1:n.2579+19T>C
XM_017028502.1:c.2579+19T>C	XP_016883991.1:n.2579+19T>C
XM_017028503.1:c.2579+19T>C	XP_016883992.1:n.2579+19T>C
XM_017028504.1:c.2579+19T>C	XP_016883993.1:n.2579+19T>C
XM_017028505.2:c.2681+19T>C	XP_016883994.1:n.2681+19T>C
NM_001160306.2:c.2564+19T>C	NP_001153778.1:n.2564+19T>C
NM_203446.3:c.2579+19T>C MANE Select	NP_982271.3:n.2579+19T>C